Canonical Allele Identifier: CA422513372

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.185963996T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185994864T>A , CM000663.2:g.185994864T>A	GRCh38
NC_000001.10:g.185963996T>A , CM000663.1:g.185963996T>A	GRCh37
NC_000001.9:g.184230619T>A	NCBI36
NG_011841.1:g.265314T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.3555T>A MANE Select	ENSP00000271588.4:p.Gly1185=
ENST00000271588.8:c.3555T>A	ENSP00000271588.4:p.Gly1185=
NM_031935.2:c.3555T>A	NP_114141.2:p.Gly1185=
XM_011510037.1:c.3555T>A	XP_011508339.1:p.Gly1185=
XM_011510038.1:c.3555T>A	XP_011508340.1:p.Gly1185=
XM_011510039.1:c.3555T>A	XP_011508341.1:p.Gly1185=
XM_011510040.1:c.3555T>A	XP_011508342.1:p.Gly1185=
XM_011510041.1:c.3555T>A	XP_011508343.1:p.Gly1185=
XM_011510038.3:c.3555T>A	XP_011508340.1:p.Gly1185=
XM_011510041.3:c.3555T>A	XP_011508343.1:p.Gly1185=
XM_017002437.1:c.1578T>A	XP_016857926.1:p.Gly526=
XM_024450118.1:c.3555T>A	XP_024305886.1:p.Gly1185=
NM_031935.3:c.3555T>A MANE Select	NP_114141.2:p.Gly1185=