Canonical Allele Identifier: CA1770267676
Gene: HR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22123634_22123636delinsCAG , CM000670.2:g.22123634_22123636delinsCAG GRCh38
NC_000008.10:g.21981147_21981149delinsCAG , CM000670.1:g.21981147_21981149delinsCAG GRCh37
NC_000008.9:g.22037092_22037094delinsCAG NCBI36
NG_008166.1:g.11882_11884delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000381418.9:c.1915+13_1915+15delinsCTG MANE Select ENSP00000370826.4:n.1915+13_1915+15delins...
ENST00000680789.1:c.1915+13_1915+15delinsCTG ENSP00000505181.1:n.1915+13_1915+15delins...
ENST00000312841.9:c.1915+13_1915+15delinsCTG ENSP00000326765.8:n.1915+13_1915+15delins...
ENST00000381418.8:c.1915+13_1915+15delinsCTG ENSP00000370826.4:n.1915+13_1915+15delins...
NM_005144.4:c.1915+13_1915+15delinsCTG NP_005135.2:n.1915+13_1915+15delinsCTG
NM_018411.4:c.1915+13_1915+15delinsCTG NP_060881.2:n.1915+13_1915+15delinsCTG
XM_005273569.1:c.1918+13_1918+15delinsCTG XP_005273626.1:n.1918+13_1918+15delinsCTG...
XM_006716367.1:c.1918+13_1918+15delinsCTG XP_006716430.1:n.1918+13_1918+15delinsCTG...
XM_005273569.2:c.1918+13_1918+15delinsCTG XP_005273626.1:n.1918+13_1918+15delinsCTG...
XM_006716367.2:c.1918+13_1918+15delinsCTG XP_006716430.1:n.1918+13_1918+15delinsCTG...
NM_005144.5:c.1915+13_1915+15delinsCTG MANE Select NP_005135.2:n.1915+13_1915+15delinsCTG