Canonical Allele Identifier: CA1592792887

Gene: HAND1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154477446A= , CM000667.2:g.154477446A=	GRCh38
NC_000005.9:g.153857006A= , CM000667.1:g.153857006A=	GRCh37
NC_000005.8:g.153837199A=	NCBI36
NG_052889.1:g.5819T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231121.3:c.543+20T= MANE Select	ENSP00000231121.2:n.543+20T=
ENST00000231121.2:c.543+20T=	ENSP00000231121.2:n.543+20T=
NM_004821.2:c.543+20T=	NP_004812.1:n.543+20T=
XM_005268531.1:c.543+20T=	XP_005268588.1:n.543+20T=
NM_004821.3:c.543+20T= MANE Select	NP_004812.1:n.543+20T=