Canonical Allele Identifier: CA7963572

Gene: PALB2

Linked Data

• dbSNP Id: rs746802428
• ExAC: 16:23641032 A / T
• gnomAD v2: 16-23641032-A-T
• gnomAD v4: 16-23629711-A-T
• MyVariant Identifiers: chr16:g.23641032A>T (hg19) ; chr16:g.23629711A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629711A>T , CM000678.2:g.23629711A>T	GRCh38
NC_000016.9:g.23641032A>T , CM000678.1:g.23641032A>T	GRCh37
NC_000016.8:g.23548533A>T	NCBI36
NG_007406.1:g.16647T>A , LRG_308:g.16647T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2449T>A	ENSP00000460666.3:p.Ser817Thr
ENST00000565038.2:c.212-436T>A	ENSP00000459882.2:n.212-436T>A
ENST00000566069.6:c.2443T>A	ENSP00000459237.2:p.Ser815Thr
ENST00000697377.2:c.2449T>A	ENSP00000513286.2:p.Ser817Thr
ENST00000697379.2:c.2449T>A	ENSP00000513287.2:p.Ser817Thr
ENST00000561514.2:c.1558T>A	ENSP00000460666.2:p.Ser520Thr
ENST00000697374.1:c.1558T>A	ENSP00000513284.1:p.Ser520Thr
ENST00000697375.1:n.3790T>A
ENST00000697376.1:c.1558T>A	ENSP00000513285.1:p.Ser520Thr
ENST00000697377.1:c.1558T>A	ENSP00000513286.1:p.Ser520Thr
ENST00000697378.1:n.2963T>A
ENST00000697379.1:c.1558T>A	ENSP00000513287.1:p.Ser520Thr
ENST00000697380.1:n.1371T>A
ENST00000697381.1:n.1138T>A
ENST00000697382.1:c.1558T>A	ENSP00000513288.1:p.Ser520Thr
ENST00000697383.1:c.49-436T>A	ENSP00000513289.1:n.49-436T>A
ENST00000697384.1:n.2597T>A
ENST00000261584.9:c.2443T>A MANE Select	ENSP00000261584.4:p.Ser815Thr
ENST00000261584.8:c.2443T>A	ENSP00000261584.4:p.Ser815Thr
ENST00000565038.1:c.87-436T>A
ENST00000568219.5:c.1558T>A	ENSP00000454703.2:p.Ser520Thr
NM_024675.3:c.2443T>A , LRG_308t1:c.2443T>A	NP_078951.2:p.Ser815Thr
XM_011545946.1:c.2449T>A	XP_011544248.1:p.Ser817Thr
XM_011545947.1:c.2449T>A	XP_011544249.1:p.Ser817Thr
XM_011545948.1:c.1558T>A	XP_011544250.1:p.Ser520Thr
XR_950851.1:n.3239T>A
XM_011545946.2:c.2449T>A	XP_011544248.1:p.Ser817Thr
XM_011545947.2:c.2449T>A	XP_011544249.1:p.Ser817Thr
XM_011545948.2:c.1558T>A	XP_011544250.1:p.Ser520Thr
XM_017023671.1:c.2449T>A	XP_016879160.1:p.Ser817Thr
XM_017023672.2:c.2443T>A	XP_016879161.1:p.Ser815Thr
XM_017023673.2:c.2443T>A	XP_016879162.1:p.Ser815Thr
NM_024675.4:c.2443T>A MANE Select	NP_078951.2:p.Ser815Thr