Canonical Allele Identifier: CA395144149

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23634353A>C (hg19) ; chr16:g.23623032A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623032A>C , CM000678.2:g.23623032A>C	GRCh38
NC_000016.9:g.23634353A>C , CM000678.1:g.23634353A>C	GRCh37
NC_000016.8:g.23541854A>C	NCBI36
NG_007406.1:g.23326T>G , LRG_308:g.23326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2939T>G	ENSP00000460666.3:p.Val980Gly
ENST00000565038.2:c.*414T>G	ENSP00000459882.2:n.*414T>G
ENST00000566069.6:c.2933T>G	ENSP00000459237.2:p.Val978Gly
ENST00000697377.2:c.2777T>G	ENSP00000513286.2:p.Val926Gly
ENST00000697379.2:c.2939T>G	ENSP00000513287.2:p.Val980Gly
ENST00000561514.2:c.2048T>G	ENSP00000460666.2:p.Val683Gly
ENST00000697374.1:c.2048T>G	ENSP00000513284.1:p.Val683Gly
ENST00000697375.1:n.4280T>G
ENST00000697376.1:c.2048T>G	ENSP00000513285.1:p.Val683Gly
ENST00000697377.1:c.1886T>G	ENSP00000513286.1:p.Val629Gly
ENST00000697378.1:n.3453T>G
ENST00000697379.1:c.2048T>G	ENSP00000513287.1:p.Val683Gly
ENST00000697380.1:n.2225T>G
ENST00000697381.1:n.1628T>G
ENST00000697382.1:c.2048T>G	ENSP00000513288.1:p.Val683Gly
ENST00000697383.1:c.467T>G	ENSP00000513289.1:p.Val156Gly
ENST00000261584.9:c.2933T>G MANE Select	ENSP00000261584.4:p.Val978Gly
ENST00000261584.8:c.2933T>G	ENSP00000261584.4:p.Val978Gly
ENST00000568219.5:c.2048T>G	ENSP00000454703.2:p.Val683Gly
NM_024675.3:c.2933T>G , LRG_308t1:c.2933T>G	NP_078951.2:p.Val978Gly
XM_011545946.1:c.2939T>G	XP_011544248.1:p.Val980Gly
XM_011545947.1:c.2939T>G	XP_011544249.1:p.Val980Gly
XM_011545948.1:c.2048T>G	XP_011544250.1:p.Val683Gly
XR_950851.1:n.3729T>G
XM_011545946.2:c.2939T>G	XP_011544248.1:p.Val980Gly
XM_011545947.2:c.2939T>G	XP_011544249.1:p.Val980Gly
XM_011545948.2:c.2048T>G	XP_011544250.1:p.Val683Gly
XM_017023671.1:c.2939T>G	XP_016879160.1:p.Val980Gly
XM_017023672.2:c.2933T>G	XP_016879161.1:p.Val978Gly
XM_017023673.2:c.2933T>G	XP_016879162.1:p.Val978Gly
NM_024675.4:c.2933T>G MANE Select	NP_078951.2:p.Val978Gly