Canonical Allele Identifier: CA1770271745

Gene: HR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22125565_22125566delinsCA , CM000670.2:g.22125565_22125566delinsCA	GRCh38
NC_000008.10:g.21983078_21983079delinsCA , CM000670.1:g.21983078_21983079delinsCA	GRCh37
NC_000008.9:g.22039023_22039024delinsCA	NCBI36
NG_008166.1:g.9952_9953delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.1556+16_1556+17delinsTG MANE Select	ENSP00000370826.4:n.1556+16_1556+17delinsTG
ENST00000680789.1:c.1556+16_1556+17delinsTG	ENSP00000505181.1:n.1556+16_1556+17delinsTG
ENST00000312841.9:c.1556+16_1556+17delinsTG	ENSP00000326765.8:n.1556+16_1556+17delinsTG
ENST00000381418.8:c.1556+16_1556+17delinsTG	ENSP00000370826.4:n.1556+16_1556+17delinsTG
NM_005144.4:c.1556+16_1556+17delinsTG	NP_005135.2:n.1556+16_1556+17delinsTG
NM_018411.4:c.1556+16_1556+17delinsTG	NP_060881.2:n.1556+16_1556+17delinsTG
XM_005273569.1:c.1556+16_1556+17delinsTG	XP_005273626.1:n.1556+16_1556+17delinsTG
XM_006716367.1:c.1556+16_1556+17delinsTG	XP_006716430.1:n.1556+16_1556+17delinsTG
XM_005273569.2:c.1556+16_1556+17delinsTG	XP_005273626.1:n.1556+16_1556+17delinsTG
XM_006716367.2:c.1556+16_1556+17delinsTG	XP_006716430.1:n.1556+16_1556+17delinsTG
NM_005144.5:c.1556+16_1556+17delinsTG MANE Select	NP_005135.2:n.1556+16_1556+17delinsTG