Canonical Allele Identifier: CA1592792947
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477485C= , CM000667.2:g.154477485C= GRCh38
NC_000005.9:g.153857045C= , CM000667.1:g.153857045C= GRCh37
NC_000005.8:g.153837238C= NCBI36
NG_052889.1:g.5780G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.524G= MANE Select ENSP00000231121.2:p.Ser175=
ENST00000231121.2:c.524G= ENSP00000231121.2:p.Ser175=
NM_004821.2:c.524G= NP_004812.1:p.Ser175=
XM_005268531.1:c.524G= XP_005268588.1:p.Ser175=
NM_004821.3:c.524G= MANE Select NP_004812.1:p.Ser175=