Canonical Allele Identifier: CA2213428738
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23607866G= , CM000678.2:g.23607866G= GRCh38
NC_000016.9:g.23619187G= , CM000678.1:g.23619187G= GRCh37
NC_000016.8:g.23526688G= NCBI36
NG_007406.1:g.38492C= , LRG_308:g.38492C=

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3354C= ENSP00000460666.3:p.Gly1118=
ENST00000565038.2:c.*829C= ENSP00000459882.2:n.*829C=
ENST00000566069.6:c.3202-4197C= ENSP00000459237.2:n.3202-4197C=
ENST00000697377.2:c.3192C= ENSP00000513286.2:p.Gly1064=
ENST00000697379.2:c.3354C= ENSP00000513287.2:p.Gly1118=
ENST00000561514.2:c.2463C= ENSP00000460666.2:p.Gly821=
ENST00000697374.1:c.2463C= ENSP00000513284.1:p.Gly821=
ENST00000697375.1:n.4695C=
ENST00000697376.1:c.2317-4197C= ENSP00000513285.1:n.2317-4197C=
ENST00000697377.1:c.2301C= ENSP00000513286.1:p.Gly767=
ENST00000697378.1:n.3868C=
ENST00000697379.1:c.2463C= ENSP00000513287.1:p.Gly821=
ENST00000697380.1:n.2552C=
ENST00000697381.1:n.2043C=
ENST00000697382.1:c.*125C= ENSP00000513288.1:n.*125C=
ENST00000697383.1:c.882C= ENSP00000513289.1:p.Gly294=
ENST00000261584.9:c.3348C= MANE Select ENSP00000261584.4:p.Gly1116=
ENST00000261584.8:c.3348C= ENSP00000261584.4:p.Gly1116=
ENST00000566069.5:c.117-4197C=
ENST00000568219.5:c.2463C= ENSP00000454703.2:p.Gly821=
NM_024675.3:c.3348C= , LRG_308t1:c.3348C= NP_078951.2:p.Gly1116=
XM_011545946.1:c.3354C= XP_011544248.1:p.Gly1118=
XM_011545947.1:c.3208-4197C= XP_011544249.1:n.3208-4197C=
XM_011545948.1:c.2463C= XP_011544250.1:p.Gly821=
XR_950851.1:n.4056C=
XM_011545946.2:c.3354C= XP_011544248.1:p.Gly1118=
XM_011545947.2:c.3208-4197C= XP_011544249.1:n.3208-4197C=
XM_011545948.2:c.2463C= XP_011544250.1:p.Gly821=
XM_017023671.1:c.3120-4197C= XP_016879160.1:n.3120-4197C=
XM_017023672.2:c.3114-4197C= XP_016879161.1:n.3114-4197C=
XM_017023673.2:c.3202-4197C= XP_016879162.1:n.3202-4197C=
NM_024675.4:c.3348C= MANE Select NP_078951.2:p.Gly1116=