Canonical Allele Identifier: CA343870905

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.185964003G>C (hg19) ; chr1:g.185994871G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185994871G>C , CM000663.2:g.185994871G>C	GRCh38
NC_000001.10:g.185964003G>C , CM000663.1:g.185964003G>C	GRCh37
NC_000001.9:g.184230626G>C	NCBI36
NG_011841.1:g.265321G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.3562G>C MANE Select	ENSP00000271588.4:p.Val1188Leu
ENST00000271588.8:c.3562G>C	ENSP00000271588.4:p.Val1188Leu
NM_031935.2:c.3562G>C	NP_114141.2:p.Val1188Leu
XM_011510037.1:c.3562G>C	XP_011508339.1:p.Val1188Leu
XM_011510038.1:c.3562G>C	XP_011508340.1:p.Val1188Leu
XM_011510039.1:c.3562G>C	XP_011508341.1:p.Val1188Leu
XM_011510040.1:c.3562G>C	XP_011508342.1:p.Val1188Leu
XM_011510041.1:c.3562G>C	XP_011508343.1:p.Val1188Leu
XM_011510038.3:c.3562G>C	XP_011508340.1:p.Val1188Leu
XM_011510041.3:c.3562G>C	XP_011508343.1:p.Val1188Leu
XM_017002437.1:c.1585G>C	XP_016857926.1:p.Val529Leu
XM_024450118.1:c.3562G>C	XP_024305886.1:p.Val1188Leu
NM_031935.3:c.3562G>C MANE Select	NP_114141.2:p.Val1188Leu