Canonical Allele Identifier: CA2213409544
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621322_23621323delinsCT , CM000678.2:g.23621322_23621323delinsCT GRCh38
NC_000016.9:g.23632643_23632644delinsCT , CM000678.1:g.23632643_23632644delinsCT GRCh37
NC_000016.8:g.23540144_23540145delinsCT NCBI36
NG_007406.1:g.25035_25036delinsAG , LRG_308:g.25035_25036delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3119+39_3119+40delinsAG ENSP00000460666.3:n.3119+39_3119+40delinsAG
ENST00000565038.2:c.*594+39_*594+40delinsAG ENSP00000459882.2:n.*594+39_*594+40delinsAG
ENST00000566069.6:c.3113+39_3113+40delinsAG ENSP00000459237.2:n.3113+39_3113+40delinsAG
ENST00000697377.2:c.2957+39_2957+40delinsAG ENSP00000513286.2:n.2957+39_2957+40delinsAG
ENST00000697379.2:c.3119+39_3119+40delinsAG ENSP00000513287.2:n.3119+39_3119+40delinsAG
ENST00000561514.2:c.2228+39_2228+40delinsAG ENSP00000460666.2:n.2228+39_2228+40delinsAG
ENST00000697374.1:c.2228+39_2228+40delinsAG ENSP00000513284.1:n.2228+39_2228+40delinsAG
ENST00000697375.1:n.4460+39_4460+40delinsAG
ENST00000697376.1:c.2228+39_2228+40delinsAG ENSP00000513285.1:n.2228+39_2228+40delinsAG
ENST00000697377.1:c.2066+39_2066+40delinsAG ENSP00000513286.1:n.2066+39_2066+40delinsAG
ENST00000697378.1:n.3633+39_3633+40delinsAG
ENST00000697379.1:c.2228+39_2228+40delinsAG ENSP00000513287.1:n.2228+39_2228+40delinsAG
ENST00000697380.1:n.2405+39_2405+40delinsAG
ENST00000697381.1:n.1808+39_1808+40delinsAG
ENST00000697382.1:c.2228+39_2228+40delinsAG ENSP00000513288.1:n.2228+39_2228+40delinsAG
ENST00000697383.1:c.647+39_647+40delinsAG ENSP00000513289.1:n.647+39_647+40delinsAG
ENST00000261584.9:c.3113+39_3113+40delinsAG MANE Select ENSP00000261584.4:n.3113+39_3113+40delinsAG
ENST00000261584.8:c.3113+39_3113+40delinsAG ENSP00000261584.4:n.3113+39_3113+40delinsAG
ENST00000566069.5:c.28+39_28+40delinsAG
ENST00000568219.5:c.2228+39_2228+40delinsAG ENSP00000454703.2:n.2228+39_2228+40delinsAG
NM_024675.3:c.3113+39_3113+40delinsAG , LRG_308t1:c.3113+39_3113+40delinsAG NP_078951.2:n.3113+39_3113+40delinsAG
XM_011545946.1:c.3119+39_3119+40delinsAG XP_011544248.1:n.3119+39_3119+40delinsAG
XM_011545947.1:c.3119+39_3119+40delinsAG XP_011544249.1:n.3119+39_3119+40delinsAG
XM_011545948.1:c.2228+39_2228+40delinsAG XP_011544250.1:n.2228+39_2228+40delinsAG
XR_950851.1:n.3909+39_3909+40delinsAG
XM_011545946.2:c.3119+39_3119+40delinsAG XP_011544248.1:n.3119+39_3119+40delinsAG
XM_011545947.2:c.3119+39_3119+40delinsAG XP_011544249.1:n.3119+39_3119+40delinsAG
XM_011545948.2:c.2228+39_2228+40delinsAG XP_011544250.1:n.2228+39_2228+40delinsAG
XM_017023671.1:c.3119+39_3119+40delinsAG XP_016879160.1:n.3119+39_3119+40delinsAG
XM_017023672.2:c.3113+39_3113+40delinsAG XP_016879161.1:n.3113+39_3113+40delinsAG
XM_017023673.2:c.3113+39_3113+40delinsAG XP_016879162.1:n.3113+39_3113+40delinsAG
NM_024675.4:c.3113+39_3113+40delinsAG MANE Select NP_078951.2:n.3113+39_3113+40delinsAG