Canonical Allele Identifier: CA1212952014
Gene: HMCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185994761_185994765delinsTAAAG , CM000663.2:g.185994761_185994765delinsTAAAG GRCh38
NC_000001.10:g.185963893_185963897delinsTAAAG , CM000663.1:g.185963893_185963897delinsTAAAG GRCh37
NC_000001.9:g.184230516_184230520delinsTAAAG NCBI36
NG_011841.1:g.265211_265215delinsTAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.3506-54_3506-50delinsTAAAG MANE Select ENSP00000271588.4:n.3506-54_3506-50delinsTAAAG
ENST00000271588.8:c.3506-54_3506-50delinsTAAAG ENSP00000271588.4:n.3506-54_3506-50delinsTAAAG
NM_031935.2:c.3506-54_3506-50delinsTAAAG NP_114141.2:n.3506-54_3506-50delinsTAAAG
XM_011510037.1:c.3506-54_3506-50delinsTAAAG XP_011508339.1:n.3506-54_3506-50delinsTAAAG
XM_011510038.1:c.3506-54_3506-50delinsTAAAG XP_011508340.1:n.3506-54_3506-50delinsTAAAG
XM_011510039.1:c.3506-54_3506-50delinsTAAAG XP_011508341.1:n.3506-54_3506-50delinsTAAAG
XM_011510040.1:c.3506-54_3506-50delinsTAAAG XP_011508342.1:n.3506-54_3506-50delinsTAAAG
XM_011510041.1:c.3506-54_3506-50delinsTAAAG XP_011508343.1:n.3506-54_3506-50delinsTAAAG
XM_011510038.3:c.3506-54_3506-50delinsTAAAG XP_011508340.1:n.3506-54_3506-50delinsTAAAG
XM_011510041.3:c.3506-54_3506-50delinsTAAAG XP_011508343.1:n.3506-54_3506-50delinsTAAAG
XM_017002437.1:c.1529-54_1529-50delinsTAAAG XP_016857926.1:n.1529-54_1529-50delinsTAAAG
XM_024450118.1:c.3506-54_3506-50delinsTAAAG XP_024305886.1:n.3506-54_3506-50delinsTAAAG
NM_031935.3:c.3506-54_3506-50delinsTAAAG MANE Select NP_114141.2:n.3506-54_3506-50delinsTAAAG