Canonical Allele Identifier: CA2732053020

Gene: PALB2

Linked Data

• dbSNP Id: rs2142333626

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23622920A>T , CM000678.2:g.23622920A>T	GRCh38
NC_000016.9:g.23634241A>T , CM000678.1:g.23634241A>T	GRCh37
NC_000016.8:g.23541742A>T	NCBI36
NG_007406.1:g.23438T>A , LRG_308:g.23438T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3002+49T>A	ENSP00000460666.3:n.3002+49T>A
ENST00000565038.2:c.*477+49T>A	ENSP00000459882.2:n.*477+49T>A
ENST00000566069.6:c.2996+49T>A	ENSP00000459237.2:n.2996+49T>A
ENST00000697377.2:c.2840+49T>A	ENSP00000513286.2:n.2840+49T>A
ENST00000697379.2:c.3002+49T>A	ENSP00000513287.2:n.3002+49T>A
ENST00000561514.2:c.2111+49T>A	ENSP00000460666.2:n.2111+49T>A
ENST00000697374.1:c.2111+49T>A	ENSP00000513284.1:n.2111+49T>A
ENST00000697375.1:n.4343+49T>A
ENST00000697376.1:c.2111+49T>A	ENSP00000513285.1:n.2111+49T>A
ENST00000697377.1:c.1949+49T>A	ENSP00000513286.1:n.1949+49T>A
ENST00000697378.1:n.3516+49T>A
ENST00000697379.1:c.2111+49T>A	ENSP00000513287.1:n.2111+49T>A
ENST00000697380.1:n.2288+49T>A
ENST00000697381.1:n.1691+49T>A
ENST00000697382.1:c.2111+49T>A	ENSP00000513288.1:n.2111+49T>A
ENST00000697383.1:c.530+49T>A	ENSP00000513289.1:n.530+49T>A
ENST00000261584.9:c.2996+49T>A MANE Select	ENSP00000261584.4:n.2996+49T>A
ENST00000261584.8:c.2996+49T>A	ENSP00000261584.4:n.2996+49T>A
ENST00000568219.5:c.2111+49T>A	ENSP00000454703.2:n.2111+49T>A
NM_024675.3:c.2996+49T>A , LRG_308t1:c.2996+49T>A	NP_078951.2:n.2996+49T>A
XM_011545946.1:c.3002+49T>A	XP_011544248.1:n.3002+49T>A
XM_011545947.1:c.3002+49T>A	XP_011544249.1:n.3002+49T>A
XM_011545948.1:c.2111+49T>A	XP_011544250.1:n.2111+49T>A
XR_950851.1:n.3792+49T>A
XM_011545946.2:c.3002+49T>A	XP_011544248.1:n.3002+49T>A
XM_011545947.2:c.3002+49T>A	XP_011544249.1:n.3002+49T>A
XM_011545948.2:c.2111+49T>A	XP_011544250.1:n.2111+49T>A
XM_017023671.1:c.3002+49T>A	XP_016879160.1:n.3002+49T>A
XM_017023672.2:c.2996+49T>A	XP_016879161.1:n.2996+49T>A
XM_017023673.2:c.2996+49T>A	XP_016879162.1:n.2996+49T>A
NM_024675.4:c.2996+49T>A MANE Select	NP_078951.2:n.2996+49T>A