Canonical Allele Identifier: CA2213409619
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621357_23621358delinsCT , CM000678.2:g.23621357_23621358delinsCT GRCh38
NC_000016.9:g.23632678_23632679delinsCT , CM000678.1:g.23632678_23632679delinsCT GRCh37
NC_000016.8:g.23540179_23540180delinsCT NCBI36
NG_007406.1:g.25000_25001delinsAG , LRG_308:g.25000_25001delinsAG

Transcript Alleles

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