Canonical Allele Identifier: CA1213024959

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186166810_186166811delinsAT , CM000663.2:g.186166810_186166811delinsAT	GRCh38
NC_000001.10:g.186135942_186135943delinsAT , CM000663.1:g.186135942_186135943delinsAT	GRCh37
NC_000001.9:g.184402565_184402566delinsAT	NCBI36
NG_011841.1:g.437260_437261delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15442_15443delinsAT MANE Select	ENSP00000271588.4:p.Ile5148=
ENST00000271588.8:c.15442_15443delinsAT	ENSP00000271588.4:p.Ile5148=
ENST00000475585.1:n.163-4527_163-4526delinsAT
NM_031935.2:c.15442_15443delinsAT	NP_114141.2:p.Ile5148=
XM_011510037.1:c.15157_15158delinsAT	XP_011508339.1:p.Ile5053=
XM_011510038.1:c.15442_15443delinsAT	XP_011508340.1:p.Ile5148=
XM_011510038.3:c.15442_15443delinsAT	XP_011508340.1:p.Ile5148=
XM_017002437.1:c.13465_13466delinsAT	XP_016857926.1:p.Ile4489=
NM_031935.3:c.15442_15443delinsAT MANE Select	NP_114141.2:p.Ile5148=