Canonical Allele Identifier: CA2649560640

Gene: HMCN1

Linked Data

• gnomAD v4: 1-186122855-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186122855C>A , CM000663.2:g.186122855C>A	GRCh38
NC_000001.10:g.186091987C>A , CM000663.1:g.186091987C>A	GRCh37
NC_000001.9:g.184358610C>A	NCBI36
NG_011841.1:g.393305C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.12230-96C>A MANE Select	ENSP00000271588.4:n.12230-96C>A
ENST00000271588.8:c.12230-96C>A	ENSP00000271588.4:n.12230-96C>A
NM_031935.2:c.12230-96C>A	NP_114141.2:n.12230-96C>A
XM_011510037.1:c.11945-96C>A	XP_011508339.1:n.11945-96C>A
XM_011510038.1:c.12230-96C>A	XP_011508340.1:n.12230-96C>A
XM_011510039.1:c.12230-96C>A	XP_011508341.1:n.12230-96C>A
XM_011510038.3:c.12230-96C>A	XP_011508340.1:n.12230-96C>A
XM_017002437.1:c.10253-96C>A	XP_016857926.1:n.10253-96C>A
NM_031935.3:c.12230-96C>A MANE Select	NP_114141.2:n.12230-96C>A