Canonical Allele Identifier: CA343931422

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.186064624T>G (hg19) ; chr1:g.186095492T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186095492T>G , CM000663.2:g.186095492T>G	GRCh38
NC_000001.10:g.186064624T>G , CM000663.1:g.186064624T>G	GRCh37
NC_000001.9:g.184331247T>G	NCBI36
NG_011841.1:g.365942T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.10544T>G MANE Select	ENSP00000271588.4:p.Val3515Gly
ENST00000271588.8:c.10544T>G	ENSP00000271588.4:p.Val3515Gly
NM_031935.2:c.10544T>G	NP_114141.2:p.Val3515Gly
XM_011510037.1:c.10259T>G	XP_011508339.1:p.Val3420Gly
XM_011510038.1:c.10544T>G	XP_011508340.1:p.Val3515Gly
XM_011510039.1:c.10544T>G	XP_011508341.1:p.Val3515Gly
XM_011510038.3:c.10544T>G	XP_011508340.1:p.Val3515Gly
XM_017002437.1:c.8567T>G	XP_016857926.1:p.Val2856Gly
NM_031935.3:c.10544T>G MANE Select	NP_114141.2:p.Val3515Gly