Canonical Allele Identifier: CA1292413

Gene: HMCN1

Linked Data

• ClinVar Variation Id: 294166
• ClinVar RCV Id: RCV000272357 ; RCV000964239
• dbSNP Id: rs144649977
• ExAC: 1:186007997 G / T
• gnomAD v2: 1-186007997-G-T
• gnomAD v3: 1-186038865-G-T
• gnomAD v4: 1-186038865-G-T
• MyVariant Identifiers: chr1:g.186007997G>T (hg19) ; chr1:g.186038865G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186038865G>T , CM000663.2:g.186038865G>T	GRCh38
NC_000001.10:g.186007997G>T , CM000663.1:g.186007997G>T	GRCh37
NC_000001.9:g.184274620G>T	NCBI36
NG_011841.1:g.309315G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.5888G>T MANE Select	ENSP00000271588.4:p.Gly1963Val
ENST00000271588.8:c.5888G>T	ENSP00000271588.4:p.Gly1963Val
NM_031935.2:c.5888G>T	NP_114141.2:p.Gly1963Val
XM_011510037.1:c.5888G>T	XP_011508339.1:p.Gly1963Val
XM_011510038.1:c.5888G>T	XP_011508340.1:p.Gly1963Val
XM_011510039.1:c.5888G>T	XP_011508341.1:p.Gly1963Val
XM_011510040.1:c.5888G>T	XP_011508342.1:p.Gly1963Val
XM_011510041.1:c.5888G>T	XP_011508343.1:p.Gly1963Val
XM_011510038.3:c.5888G>T	XP_011508340.1:p.Gly1963Val
XM_011510041.3:c.5888G>T	XP_011508343.1:p.Gly1963Val
XM_017002437.1:c.3911G>T	XP_016857926.1:p.Gly1304Val
XM_024450118.1:c.5888G>T	XP_024305886.1:p.Gly1963Val
NM_031935.3:c.5888G>T MANE Select	NP_114141.2:p.Gly1963Val