Canonical Allele Identifier: CA395125636

Gene: PALB2

Linked Data

• dbSNP Id: rs1555460459
• MyVariant Identifiers: chr16:g.23641296C>T (hg19) ; chr16:g.23629975C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629975C>T , CM000678.2:g.23629975C>T	GRCh38
NC_000016.9:g.23641296C>T , CM000678.1:g.23641296C>T	GRCh37
NC_000016.8:g.23548797C>T	NCBI36
NG_007406.1:g.16383G>A , LRG_308:g.16383G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2185G>A	ENSP00000460666.3:p.Ala729Thr
ENST00000565038.2:c.212-700G>A	ENSP00000459882.2:n.212-700G>A
ENST00000566069.6:c.2179G>A	ENSP00000459237.2:p.Ala727Thr
ENST00000697377.2:c.2185G>A	ENSP00000513286.2:p.Ala729Thr
ENST00000697379.2:c.2185G>A	ENSP00000513287.2:p.Ala729Thr
ENST00000561514.2:c.1294G>A	ENSP00000460666.2:p.Ala432Thr
ENST00000697374.1:c.1294G>A	ENSP00000513284.1:p.Ala432Thr
ENST00000697375.1:n.3526G>A
ENST00000697376.1:c.1294G>A	ENSP00000513285.1:p.Ala432Thr
ENST00000697377.1:c.1294G>A	ENSP00000513286.1:p.Ala432Thr
ENST00000697378.1:n.2699G>A
ENST00000697379.1:c.1294G>A	ENSP00000513287.1:p.Ala432Thr
ENST00000697380.1:n.1107G>A
ENST00000697381.1:n.874G>A
ENST00000697382.1:c.1294G>A	ENSP00000513288.1:p.Ala432Thr
ENST00000697383.1:c.49-700G>A	ENSP00000513289.1:n.49-700G>A
ENST00000697384.1:n.2333G>A
ENST00000261584.9:c.2179G>A MANE Select	ENSP00000261584.4:p.Ala727Thr
ENST00000261584.8:c.2179G>A	ENSP00000261584.4:p.Ala727Thr
ENST00000565038.1:c.87-700G>A
ENST00000568219.5:c.1294G>A	ENSP00000454703.2:p.Ala432Thr
NM_024675.3:c.2179G>A , LRG_308t1:c.2179G>A	NP_078951.2:p.Ala727Thr
XM_011545946.1:c.2185G>A	XP_011544248.1:p.Ala729Thr
XM_011545947.1:c.2185G>A	XP_011544249.1:p.Ala729Thr
XM_011545948.1:c.1294G>A	XP_011544250.1:p.Ala432Thr
XR_950851.1:n.2975G>A
XM_011545946.2:c.2185G>A	XP_011544248.1:p.Ala729Thr
XM_011545947.2:c.2185G>A	XP_011544249.1:p.Ala729Thr
XM_011545948.2:c.1294G>A	XP_011544250.1:p.Ala432Thr
XM_017023671.1:c.2185G>A	XP_016879160.1:p.Ala729Thr
XM_017023672.2:c.2179G>A	XP_016879161.1:p.Ala727Thr
XM_017023673.2:c.2179G>A	XP_016879162.1:p.Ala727Thr
NM_024675.4:c.2179G>A MANE Select	NP_078951.2:p.Ala727Thr