Canonical Allele Identifier: CA1770267732

Gene: HR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22123645_22123647delinsCTA , CM000670.2:g.22123645_22123647delinsCTA	GRCh38
NC_000008.10:g.21981158_21981160delinsCTA , CM000670.1:g.21981158_21981160delinsCTA	GRCh37
NC_000008.9:g.22037103_22037105delinsCTA	NCBI36
NG_008166.1:g.11871_11873delinsTAG

Transcript Alleles

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