Canonical Allele Identifier: CA343870049

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.185962388T>A (hg19) ; chr1:g.185993256T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185993256T>A , CM000663.2:g.185993256T>A	GRCh38
NC_000001.10:g.185962388T>A , CM000663.1:g.185962388T>A	GRCh37
NC_000001.9:g.184229011T>A	NCBI36
NG_011841.1:g.263706T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.3452T>A MANE Select	ENSP00000271588.4:p.Val1151Asp
ENST00000271588.8:c.3452T>A	ENSP00000271588.4:p.Val1151Asp
ENST00000485744.5:n.1703T>A
NM_031935.2:c.3452T>A	NP_114141.2:p.Val1151Asp
XM_011510037.1:c.3452T>A	XP_011508339.1:p.Val1151Asp
XM_011510038.1:c.3452T>A	XP_011508340.1:p.Val1151Asp
XM_011510039.1:c.3452T>A	XP_011508341.1:p.Val1151Asp
XM_011510040.1:c.3452T>A	XP_011508342.1:p.Val1151Asp
XM_011510041.1:c.3452T>A	XP_011508343.1:p.Val1151Asp
XM_011510038.3:c.3452T>A	XP_011508340.1:p.Val1151Asp
XM_011510041.3:c.3452T>A	XP_011508343.1:p.Val1151Asp
XM_017002437.1:c.1475T>A	XP_016857926.1:p.Val492Asp
XM_024450118.1:c.3452T>A	XP_024305886.1:p.Val1151Asp
NM_031935.3:c.3452T>A MANE Select	NP_114141.2:p.Val1151Asp