Canonical Allele Identifier: CA2768994030
Gene: HAND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477356del , CM000667.2:g.154477356del GRCh38
NC_000005.9:g.153856916del , CM000667.1:g.153856916del GRCh37
NC_000005.8:g.153837109del NCBI36
NG_052889.1:g.5910del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+111del MANE Select ENSP00000231121.2:n.543+111del
ENST00000231121.2:c.543+111del ENSP00000231121.2:n.543+111del
NM_004821.2:c.543+111del NP_004812.1:n.543+111del
XM_005268531.1:c.543+111del XP_005268588.1:n.543+111del
NM_004821.3:c.543+111del MANE Select NP_004812.1:n.543+111del