Canonical Allele Identifier: CA2746980145

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186095486del , CM000663.2:g.186095486del	GRCh38
NC_000001.10:g.186064618del , CM000663.1:g.186064618del	GRCh37
NC_000001.9:g.184331241del	NCBI36
NG_011841.1:g.365936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.10538del MANE Select	ENSP00000271588.4:p.Gly3513GlufsTer12
ENST00000271588.8:c.10538del	ENSP00000271588.4:p.Gly3513GlufsTer12
NM_031935.2:c.10538del	NP_114141.2:p.Gly3513GlufsTer12
XM_011510037.1:c.10253del	XP_011508339.1:p.Gly3418GlufsTer12
XM_011510038.1:c.10538del	XP_011508340.1:p.Gly3513GlufsTer12
XM_011510039.1:c.10538del	XP_011508341.1:p.Gly3513GlufsTer12
XM_011510038.3:c.10538del	XP_011508340.1:p.Gly3513GlufsTer12
XM_017002437.1:c.8561del	XP_016857926.1:p.Gly2854GlufsTer12
NM_031935.3:c.10538del MANE Select	NP_114141.2:p.Gly3513GlufsTer12