Canonical Allele Identifier: CA1212846633

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.185734739_185734740delinsCT , CM000663.2:g.185734739_185734740delinsCT	GRCh38
NC_000001.10:g.185703871_185703872delinsCT , CM000663.1:g.185703871_185703872delinsCT	GRCh37
NC_000001.9:g.183970494_183970495delinsCT	NCBI36
NG_011841.1:g.5189_5190delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.-41_-40delinsCT MANE Select	ENSP00000271588.4:n.-41_-40delinsCT
ENST00000271588.8:c.-41_-40delinsCT	ENSP00000271588.4:n.-41_-40delinsCT
NM_031935.2:c.-41_-40delinsCT	NP_114141.2:n.-41_-40delinsCT
XM_011510037.1:c.-41_-40delinsCT	XP_011508339.1:n.-41_-40delinsCT
XM_011510038.1:c.-41_-40delinsCT	XP_011508340.1:n.-41_-40delinsCT
XM_011510039.1:c.-41_-40delinsCT	XP_011508341.1:n.-41_-40delinsCT
XM_011510040.1:c.-41_-40delinsCT	XP_011508342.1:n.-41_-40delinsCT
XM_011510041.1:c.-41_-40delinsCT	XP_011508343.1:n.-41_-40delinsCT
XM_011510038.3:c.-41_-40delinsCT	XP_011508340.1:n.-41_-40delinsCT
XM_011510041.3:c.-41_-40delinsCT	XP_011508343.1:n.-41_-40delinsCT
XM_024450118.1:c.-41_-40delinsCT	XP_024305886.1:n.-41_-40delinsCT
NM_031935.3:c.-41_-40delinsCT MANE Select	NP_114141.2:n.-41_-40delinsCT