Canonical Allele Identifier: CA1290714

Gene: HMCN1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185734755G>A , CM000663.2:g.185734755G>A	GRCh38
NC_000001.10:g.185703887G>A , CM000663.1:g.185703887G>A	GRCh37
NC_000001.9:g.183970510G>A	NCBI36
NG_011841.1:g.5205G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.-25G>A MANE Select	ENSP00000271588.4:n.-25G>A
ENST00000271588.8:c.-25G>A	ENSP00000271588.4:n.-25G>A
NM_031935.2:c.-25G>A	NP_114141.2:n.-25G>A
XM_011510037.1:c.-25G>A	XP_011508339.1:n.-25G>A
XM_011510038.1:c.-25G>A	XP_011508340.1:n.-25G>A
XM_011510039.1:c.-25G>A	XP_011508341.1:n.-25G>A
XM_011510040.1:c.-25G>A	XP_011508342.1:n.-25G>A
XM_011510041.1:c.-25G>A	XP_011508343.1:n.-25G>A
XM_011510038.3:c.-25G>A	XP_011508340.1:n.-25G>A
XM_011510041.3:c.-25G>A	XP_011508343.1:n.-25G>A
XM_024450118.1:c.-25G>A	XP_024305886.1:n.-25G>A
NM_031935.3:c.-25G>A MANE Select	NP_114141.2:n.-25G>A