Canonical Allele Identifier: CA2686436556
Gene: HR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22123618_22123619insTCCCCCCCCCCC , CM000670.2:g.22123618_22123619insTCCCCCCCCCCC GRCh38
NC_000008.10:g.21981131_21981132insTCCCCCCCCCCC , CM000670.1:g.21981131_21981132insTCCCCCCCCCCC GRCh37
NC_000008.9:g.22037076_22037077insTCCCCCCCCCCC NCBI36
NG_008166.1:g.11900_11901insGGGGGGGGGGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000381418.9:c.1915+31_1915+32insGGGGGGGGGGAG MANE Select ENSP00000370826.4:n.1915+31_1915+32insGGG...
ENST00000680789.1:c.1915+31_1915+32insGGGGGGGGGGAG ENSP00000505181.1:n.1915+31_1915+32insGGG...
ENST00000312841.9:c.1915+31_1915+32insGGGGGGGGGGAG ENSP00000326765.8:n.1915+31_1915+32insGGG...
ENST00000381418.8:c.1915+31_1915+32insGGGGGGGGGGAG ENSP00000370826.4:n.1915+31_1915+32insGGG...
NM_005144.4:c.1915+31_1915+32insGGGGGGGGGGAG NP_005135.2:n.1915+31_1915+32insGGGGGGGGG...
NM_018411.4:c.1915+31_1915+32insGGGGGGGGGGAG NP_060881.2:n.1915+31_1915+32insGGGGGGGGG...
XM_005273569.1:c.1918+31_1918+32insGGGGGGGGGGAG XP_005273626.1:n.1918+31_1918+32insGGGGGG...
XM_006716367.1:c.1918+31_1918+32insGGGGGGGGGGAG XP_006716430.1:n.1918+31_1918+32insGGGGGG...
XM_005273569.2:c.1918+31_1918+32insGGGGGGGGGGAG XP_005273626.1:n.1918+31_1918+32insGGGGGG...
XM_006716367.2:c.1918+31_1918+32insGGGGGGGGGGAG XP_006716430.1:n.1918+31_1918+32insGGGGGG...
NM_005144.5:c.1915+31_1915+32insGGGGGGGGGGAG MANE Select NP_005135.2:n.1915+31_1915+32insGGGGGGGGG...