Canonical Allele Identifier: CA1148442358

Gene: HMCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186039718_186039724delinsTTTTTTT , CM000663.2:g.186039718_186039724delinsTTTTTTT	GRCh38
NC_000001.10:g.186008850_186008856delinsTTTTTTT , CM000663.1:g.186008850_186008856delinsTTTTTTT	GRCh37
NC_000001.9:g.184275473_184275479delinsTTTTTTT	NCBI36
NG_011841.1:g.310168_310174delinsTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271588.9:c.6029-10_6029-4delinsTTTTTTT MANE Select	ENSP00000271588.4:n.6029-10_6029-4delinsTTTTTTT
ENST00000271588.8:c.6029-10_6029-4delinsTTTTTTT	ENSP00000271588.4:n.6029-10_6029-4delinsTTTTTTT
NM_031935.2:c.6029-10_6029-4delinsTTTTTTT	NP_114141.2:n.6029-10_6029-4delinsTTTTTTT
XM_011510037.1:c.6029-10_6029-4delinsTTTTTTT	XP_011508339.1:n.6029-10_6029-4delinsTTTTTTT
XM_011510038.1:c.6029-10_6029-4delinsTTTTTTT	XP_011508340.1:n.6029-10_6029-4delinsTTTTTTT
XM_011510039.1:c.6029-10_6029-4delinsTTTTTTT	XP_011508341.1:n.6029-10_6029-4delinsTTTTTTT
XM_011510040.1:c.6029-10_6029-4delinsTTTTTTT	XP_011508342.1:n.6029-10_6029-4delinsTTTTTTT
XM_011510041.1:c.6029-10_6029-4delinsTTTTTTT	XP_011508343.1:n.6029-10_6029-4delinsTTTTTTT
XM_011510038.3:c.6029-10_6029-4delinsTTTTTTT	XP_011508340.1:n.6029-10_6029-4delinsTTTTTTT
XM_011510041.3:c.6029-10_6029-4delinsTTTTTTT	XP_011508343.1:n.6029-10_6029-4delinsTTTTTTT
XM_017002437.1:c.4052-10_4052-4delinsTTTTTTT	XP_016857926.1:n.4052-10_4052-4delinsTTTTTTT
XM_024450118.1:c.6029-10_6029-4delinsTTTTTTT	XP_024305886.1:n.6029-10_6029-4delinsTTTTTTT
NM_031935.3:c.6029-10_6029-4delinsTTTTTTT MANE Select	NP_114141.2:n.6029-10_6029-4delinsTTTTTTT