Canonical Allele Identifier: CA2686436771
Gene: HR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22123629_22123630insGTG , CM000670.2:g.22123629_22123630insGTG GRCh38
NC_000008.10:g.21981142_21981143insGTG , CM000670.1:g.21981142_21981143insGTG GRCh37
NC_000008.9:g.22037087_22037088insGTG NCBI36
NG_008166.1:g.11888_11889insCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000381418.9:c.1915+19_1915+20insCAC MANE Select ENSP00000370826.4:n.1915+19_1915+20insCAC...
ENST00000680789.1:c.1915+19_1915+20insCAC ENSP00000505181.1:n.1915+19_1915+20insCAC...
ENST00000312841.9:c.1915+19_1915+20insCAC ENSP00000326765.8:n.1915+19_1915+20insCAC...
ENST00000381418.8:c.1915+19_1915+20insCAC ENSP00000370826.4:n.1915+19_1915+20insCAC...
NM_005144.4:c.1915+19_1915+20insCAC NP_005135.2:n.1915+19_1915+20insCAC
NM_018411.4:c.1915+19_1915+20insCAC NP_060881.2:n.1915+19_1915+20insCAC
XM_005273569.1:c.1918+19_1918+20insCAC XP_005273626.1:n.1918+19_1918+20insCAC
XM_006716367.1:c.1918+19_1918+20insCAC XP_006716430.1:n.1918+19_1918+20insCAC
XM_005273569.2:c.1918+19_1918+20insCAC XP_005273626.1:n.1918+19_1918+20insCAC
XM_006716367.2:c.1918+19_1918+20insCAC XP_006716430.1:n.1918+19_1918+20insCAC
NM_005144.5:c.1915+19_1915+20insCAC MANE Select NP_005135.2:n.1915+19_1915+20insCAC