Canonical Allele Identifier: CA1140561791

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186166811_186166812delinsTT , CM000663.2:g.186166811_186166812delinsTT	GRCh38
NC_000001.10:g.186135943_186135944delinsTT , CM000663.1:g.186135943_186135944delinsTT	GRCh37
NC_000001.9:g.184402566_184402567delinsTT	NCBI36
NG_011841.1:g.437261_437262delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15443_15444delinsTT MANE Select	ENSP00000271588.4:p.Ile5148=
ENST00000271588.8:c.15443_15444delinsTT	ENSP00000271588.4:p.Ile5148=
ENST00000475585.1:n.163-4526_163-4525delinsTT
NM_031935.2:c.15443_15444delinsTT	NP_114141.2:p.Ile5148=
XM_011510037.1:c.15158_15159delinsTT	XP_011508339.1:p.Ile5053=
XM_011510038.1:c.15443_15444delinsTT	XP_011508340.1:p.Ile5148=
XM_011510038.3:c.15443_15444delinsTT	XP_011508340.1:p.Ile5148=
XM_017002437.1:c.13466_13467delinsTT	XP_016857926.1:p.Ile4489=
NM_031935.3:c.15443_15444delinsTT MANE Select	NP_114141.2:p.Ile5148=