Canonical Allele Identifier: CA361921608

Gene: HAND1

Linked Data

• MyVariant Identifiers: chr5:g.153857063G>C (hg19) ; chr5:g.154477503G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154477503G>C , CM000667.2:g.154477503G>C	GRCh38
NC_000005.9:g.153857063G>C , CM000667.1:g.153857063G>C	GRCh37
NC_000005.8:g.153837256G>C	NCBI36
NG_052889.1:g.5762C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231121.3:c.506C>G MANE Select	ENSP00000231121.2:p.Ala169Gly
ENST00000231121.2:c.506C>G	ENSP00000231121.2:p.Ala169Gly
NM_004821.2:c.506C>G	NP_004812.1:p.Ala169Gly
XM_005268531.1:c.506C>G	XP_005268588.1:p.Ala169Gly
NM_004821.3:c.506C>G MANE Select	NP_004812.1:p.Ala169Gly