Canonical Allele Identifier: CA1212989872

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186082787_186082790delinsTTTA , CM000663.2:g.186082787_186082790delinsTTTA	GRCh38
NC_000001.10:g.186051919_186051922delinsTTTA , CM000663.1:g.186051919_186051922delinsTTTA	GRCh37
NC_000001.9:g.184318542_184318545delinsTTTA	NCBI36
NG_011841.1:g.353237_353240delinsTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.8788-78_8788-75delinsTTTA MANE Select	ENSP00000271588.4:n.8788-78_8788-75delinsTTTA
ENST00000271588.8:c.8788-78_8788-75delinsTTTA	ENSP00000271588.4:n.8788-78_8788-75delinsTTTA
NM_031935.2:c.8788-78_8788-75delinsTTTA	NP_114141.2:n.8788-78_8788-75delinsTTTA
XM_011510037.1:c.8788-78_8788-75delinsTTTA	XP_011508339.1:n.8788-78_8788-75delinsTTTA
XM_011510038.1:c.8788-78_8788-75delinsTTTA	XP_011508340.1:n.8788-78_8788-75delinsTTTA
XM_011510039.1:c.8788-78_8788-75delinsTTTA	XP_011508341.1:n.8788-78_8788-75delinsTTTA
XM_011510040.1:c.8788-78_8788-75delinsTTTA	XP_011508342.1:n.8788-78_8788-75delinsTTTA
XM_011510041.1:c.8788-78_8788-75delinsTTTA	XP_011508343.1:n.8788-78_8788-75delinsTTTA
XM_011510038.3:c.8788-78_8788-75delinsTTTA	XP_011508340.1:n.8788-78_8788-75delinsTTTA
XM_011510041.3:c.8788-78_8788-75delinsTTTA	XP_011508343.1:n.8788-78_8788-75delinsTTTA
XM_017002437.1:c.6811-78_6811-75delinsTTTA	XP_016857926.1:n.6811-78_6811-75delinsTTTA
XM_024450118.1:c.8788-78_8788-75delinsTTTA	XP_024305886.1:n.8788-78_8788-75delinsTTTA
NM_031935.3:c.8788-78_8788-75delinsTTTA MANE Select	NP_114141.2:n.8788-78_8788-75delinsTTTA