Canonical Allele Identifier: CA2806270231
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621590_23621591insC , CM000678.2:g.23621590_23621591insC GRCh38
NC_000016.9:g.23632911_23632912insC , CM000678.1:g.23632911_23632912insC GRCh37
NC_000016.8:g.23540412_23540413insC NCBI36
NG_007406.1:g.24767_24768insG , LRG_308:g.24767_24768insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-113_3003-112insG ENSP00000460666.3:n.3003-113_3003-112insG
ENST00000565038.2:c.*478-113_*478-112insG ENSP00000459882.2:n.*478-113_*478-112insG
ENST00000566069.6:c.2997-113_2997-112insG ENSP00000459237.2:n.2997-113_2997-112insG
ENST00000697377.2:c.2841-113_2841-112insG ENSP00000513286.2:n.2841-113_2841-112insG
ENST00000697379.2:c.3003-113_3003-112insG ENSP00000513287.2:n.3003-113_3003-112insG
ENST00000561514.2:c.2112-113_2112-112insG ENSP00000460666.2:n.2112-113_2112-112insG
ENST00000697374.1:c.2112-113_2112-112insG ENSP00000513284.1:n.2112-113_2112-112insG
ENST00000697375.1:n.4344-113_4344-112insG
ENST00000697376.1:c.2112-113_2112-112insG ENSP00000513285.1:n.2112-113_2112-112insG
ENST00000697377.1:c.1950-113_1950-112insG ENSP00000513286.1:n.1950-113_1950-112insG
ENST00000697378.1:n.3517-113_3517-112insG
ENST00000697379.1:c.2112-113_2112-112insG ENSP00000513287.1:n.2112-113_2112-112insG
ENST00000697380.1:n.2289-113_2289-112insG
ENST00000697381.1:n.1692-113_1692-112insG
ENST00000697382.1:c.2112-113_2112-112insG ENSP00000513288.1:n.2112-113_2112-112insG
ENST00000697383.1:c.531-113_531-112insG ENSP00000513289.1:n.531-113_531-112insG
ENST00000261584.9:c.2997-113_2997-112insG MANE Select ENSP00000261584.4:n.2997-113_2997-112insG
ENST00000261584.8:c.2997-113_2997-112insG ENSP00000261584.4:n.2997-113_2997-112insG
ENST00000568219.5:c.2112-113_2112-112insG ENSP00000454703.2:n.2112-113_2112-112insG
NM_024675.3:c.2997-113_2997-112insG , LRG_308t1:c.2997-113_2997-112insG NP_078951.2:n.2997-113_2997-112insG
XM_011545946.1:c.3003-113_3003-112insG XP_011544248.1:n.3003-113_3003-112insG
XM_011545947.1:c.3003-113_3003-112insG XP_011544249.1:n.3003-113_3003-112insG
XM_011545948.1:c.2112-113_2112-112insG XP_011544250.1:n.2112-113_2112-112insG
XR_950851.1:n.3793-113_3793-112insG
XM_011545946.2:c.3003-113_3003-112insG XP_011544248.1:n.3003-113_3003-112insG
XM_011545947.2:c.3003-113_3003-112insG XP_011544249.1:n.3003-113_3003-112insG
XM_011545948.2:c.2112-113_2112-112insG XP_011544250.1:n.2112-113_2112-112insG
XM_017023671.1:c.3003-113_3003-112insG XP_016879160.1:n.3003-113_3003-112insG
XM_017023672.2:c.2997-113_2997-112insG XP_016879161.1:n.2997-113_2997-112insG
XM_017023673.2:c.2997-113_2997-112insG XP_016879162.1:n.2997-113_2997-112insG
NM_024675.4:c.2997-113_2997-112insG MANE Select NP_078951.2:n.2997-113_2997-112insG