Canonical Allele Identifier: CA2667172203
Gene: HGD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120650860_120650866del , CM000665.2:g.120650860_120650866del GRCh38
NC_000003.11:g.120369707_120369713del , CM000665.1:g.120369707_120369713del GRCh37
NC_000003.10:g.121852397_121852403del NCBI36
NG_011957.1:g.36616_36622del

Transcript Alleles

HGVS Amino-acid change
ENST00000283871.10:c.343-1_348del
ENST00000283871.9:c.343-1_348del
ENST00000476082.2:c.220-1_225del
ENST00000485313.5:n.451-1_456del
NM_000187.3:c.343-1_348del
XM_005247412.1:c.343-1_348del
XM_005247413.1:c.343-1_348del
XM_005247414.3:c.343-1_348del
XM_011512746.1:c.343-1_348del
XM_005247412.2:c.343-1_348del
XM_005247413.2:c.343-1_348del
XM_005247414.5:c.343-1_348del
XM_011512746.2:c.343-1_348del
XM_017006277.2:c.-81-1_-76del
NM_000187.4:c.343-1_348del