Canonical Allele Identifier: CA1592792896
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477450A= , CM000667.2:g.154477450A= GRCh38
NC_000005.9:g.153857010A= , CM000667.1:g.153857010A= GRCh37
NC_000005.8:g.153837203A= NCBI36
NG_052889.1:g.5815T=

Transcript Alleles

HGVS Amino-acid change
ENST00000231121.3:c.543+16T= MANE Select ENSP00000231121.2:n.543+16T=
ENST00000231121.2:c.543+16T= ENSP00000231121.2:n.543+16T=
NM_004821.2:c.543+16T= NP_004812.1:n.543+16T=
XM_005268531.1:c.543+16T= XP_005268588.1:n.543+16T=
NM_004821.3:c.543+16T= MANE Select NP_004812.1:n.543+16T=