Canonical Allele Identifier: CA2649561976

Gene: HMCN1

Linked Data

• gnomAD v4: 1-186174429-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186174431del , CM000663.2:g.186174431del	GRCh38
NC_000001.10:g.186143563del , CM000663.1:g.186143563del	GRCh37
NC_000001.9:g.184410186del	NCBI36
NG_011841.1:g.444881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15815-83del MANE Select	ENSP00000271588.4:n.15815-83del
ENST00000271588.8:c.15815-83del	ENSP00000271588.4:n.15815-83del
ENST00000414277.1:c.191-83del	ENSP00000406205.1:n.191-83del
NM_031935.2:c.15815-83del	NP_114141.2:n.15815-83del
XM_011510037.1:c.15530-83del	XP_011508339.1:n.15530-83del
XM_011510038.1:c.15815-83del	XP_011508340.1:n.15815-83del
XM_011510038.3:c.15815-83del	XP_011508340.1:n.15815-83del
XM_017002437.1:c.13838-83del	XP_016857926.1:n.13838-83del
NM_031935.3:c.15815-83del MANE Select	NP_114141.2:n.15815-83del