Canonical Allele Identifier: CA343902838

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.186092088C>A (hg19) ; chr1:g.186122956C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186122956C>A , CM000663.2:g.186122956C>A	GRCh38
NC_000001.10:g.186092088C>A , CM000663.1:g.186092088C>A	GRCh37
NC_000001.9:g.184358711C>A	NCBI36
NG_011841.1:g.393406C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12235C>A MANE Select	ENSP00000271588.4:p.Pro4079Thr
ENST00000271588.8:c.12235C>A	ENSP00000271588.4:p.Pro4079Thr
NM_031935.2:c.12235C>A	NP_114141.2:p.Pro4079Thr
XM_011510037.1:c.11950C>A	XP_011508339.1:p.Pro3984Thr
XM_011510038.1:c.12235C>A	XP_011508340.1:p.Pro4079Thr
XM_011510039.1:c.12235C>A	XP_011508341.1:p.Pro4079Thr
XM_011510038.3:c.12235C>A	XP_011508340.1:p.Pro4079Thr
XM_017002437.1:c.10258C>A	XP_016857926.1:p.Pro3420Thr
NM_031935.3:c.12235C>A MANE Select	NP_114141.2:p.Pro4079Thr