Canonical Allele Identifier: CA343885109

Gene: HMCN1

Linked Data

• MyVariant Identifiers: chr1:g.185984419C>G (hg19) ; chr1:g.186015287C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186015287C>G , CM000663.2:g.186015287C>G	GRCh38
NC_000001.10:g.185984419C>G , CM000663.1:g.185984419C>G	GRCh37
NC_000001.9:g.184251042C>G	NCBI36
NG_011841.1:g.285737C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.4759C>G MANE Select	ENSP00000271588.4:p.Pro1587Ala
ENST00000271588.8:c.4759C>G	ENSP00000271588.4:p.Pro1587Ala
NM_031935.2:c.4759C>G	NP_114141.2:p.Pro1587Ala
XM_011510037.1:c.4759C>G	XP_011508339.1:p.Pro1587Ala
XM_011510038.1:c.4759C>G	XP_011508340.1:p.Pro1587Ala
XM_011510039.1:c.4759C>G	XP_011508341.1:p.Pro1587Ala
XM_011510040.1:c.4759C>G	XP_011508342.1:p.Pro1587Ala
XM_011510041.1:c.4759C>G	XP_011508343.1:p.Pro1587Ala
XM_011510038.3:c.4759C>G	XP_011508340.1:p.Pro1587Ala
XM_011510041.3:c.4759C>G	XP_011508343.1:p.Pro1587Ala
XM_017002437.1:c.2782C>G	XP_016857926.1:p.Pro928Ala
XM_024450118.1:c.4759C>G	XP_024305886.1:p.Pro1587Ala
NM_031935.3:c.4759C>G MANE Select	NP_114141.2:p.Pro1587Ala