Canonical Allele Identifier: CA913071981
Gene: HMCN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.185962382del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185993252del , CM000663.2:g.185993252del GRCh38
NC_000001.10:g.185962384del , CM000663.1:g.185962384del GRCh37
NC_000001.9:g.184229007del NCBI36
NG_011841.1:g.263702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.3448del MANE Select ENSP00000271588.4:p.Cys1150ValfsTer10
ENST00000271588.8:c.3448del ENSP00000271588.4:p.Cys1150ValfsTer10
ENST00000485744.5:n.1699del
NM_031935.2:c.3448del NP_114141.2:p.Cys1150ValfsTer10
XM_011510037.1:c.3448del XP_011508339.1:p.Cys1150ValfsTer10
XM_011510038.1:c.3448del XP_011508340.1:p.Cys1150ValfsTer10
XM_011510039.1:c.3448del XP_011508341.1:p.Cys1150ValfsTer10
XM_011510040.1:c.3448del XP_011508342.1:p.Cys1150ValfsTer10
XM_011510041.1:c.3448del XP_011508343.1:p.Cys1150ValfsTer10
XM_011510038.3:c.3448del XP_011508340.1:p.Cys1150ValfsTer10
XM_011510041.3:c.3448del XP_011508343.1:p.Cys1150ValfsTer10
XM_017002437.1:c.1471del XP_016857926.1:p.Cys491ValfsTer10
XM_024450118.1:c.3448del XP_024305886.1:p.Cys1150ValfsTer10
NM_031935.3:c.3448del MANE Select NP_114141.2:p.Cys1150ValfsTer10