Canonical Allele Identifier: CA2649546782

Gene: HMCN1

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185734642G>T , CM000663.2:g.185734642G>T	GRCh38
NC_000001.10:g.185703774G>T , CM000663.1:g.185703774G>T	GRCh37
NC_000001.9:g.183970397G>T	NCBI36
NG_011841.1:g.5092G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.-138G>T MANE Select	ENSP00000271588.4:n.-138G>T
ENST00000271588.8:c.-138G>T	ENSP00000271588.4:n.-138G>T
NM_031935.2:c.-138G>T	NP_114141.2:n.-138G>T
XM_011510037.1:c.-138G>T	XP_011508339.1:n.-138G>T
XM_011510038.1:c.-138G>T	XP_011508340.1:n.-138G>T
XM_011510039.1:c.-138G>T	XP_011508341.1:n.-138G>T
XM_011510040.1:c.-138G>T	XP_011508342.1:n.-138G>T
XM_011510041.1:c.-138G>T	XP_011508343.1:n.-138G>T
XM_011510038.3:c.-138G>T	XP_011508340.1:n.-138G>T
XM_011510041.3:c.-138G>T	XP_011508343.1:n.-138G>T
XM_024450118.1:c.-138G>T	XP_024305886.1:n.-138G>T
NM_031935.3:c.-138G>T MANE Select	NP_114141.2:n.-138G>T