Canonical Allele Identifier: CA2676143177
Gene: HAND1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154477395_154477399del , CM000667.2:g.154477395_154477399del GRCh38
NC_000005.9:g.153856955_153856959del , CM000667.1:g.153856955_153856959del GRCh37
NC_000005.8:g.153837148_153837152del NCBI36
NG_052889.1:g.5866_5870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000231121.3:c.543+67_543+71del MANE Select ENSP00000231121.2:n.543+67_543+71del
ENST00000231121.2:c.543+67_543+71del ENSP00000231121.2:n.543+67_543+71del
NM_004821.2:c.543+67_543+71del NP_004812.1:n.543+67_543+71del
XM_005268531.1:c.543+67_543+71del XP_005268588.1:n.543+67_543+71del
NM_004821.3:c.543+67_543+71del MANE Select NP_004812.1:n.543+67_543+71del