Canonical Allele Identifier: CA343935031

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.186143657T>A (hg19) ; chr1:g.186174525T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186174525T>A , CM000663.2:g.186174525T>A	GRCh38
NC_000001.10:g.186143657T>A , CM000663.1:g.186143657T>A	GRCh37
NC_000001.9:g.184410280T>A	NCBI36
NG_011841.1:g.444975T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.15826T>A MANE Select	ENSP00000271588.4:p.Cys5276Ser
ENST00000271588.8:c.15826T>A	ENSP00000271588.4:p.Cys5276Ser
ENST00000414277.1:c.202T>A	ENSP00000406205.1:p.Cys68Ser
NM_031935.2:c.15826T>A	NP_114141.2:p.Cys5276Ser
XM_011510037.1:c.15541T>A	XP_011508339.1:p.Cys5181Ser
XM_011510038.1:c.15826T>A	XP_011508340.1:p.Cys5276Ser
XM_011510038.3:c.15826T>A	XP_011508340.1:p.Cys5276Ser
XM_017002437.1:c.13849T>A	XP_016857926.1:p.Cys4617Ser
NM_031935.3:c.15826T>A MANE Select	NP_114141.2:p.Cys5276Ser