Canonical Allele Identifier: CA1770254758

Gene: HR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116510_22116513delinsCTAA , CM000670.2:g.22116510_22116513delinsCTAA	GRCh38
NC_000008.10:g.21974023_21974026delinsCTAA , CM000670.1:g.21974023_21974026delinsCTAA	GRCh37
NC_000008.9:g.22029968_22029971delinsCTAA	NCBI36
NG_008166.1:g.19005_19008delinsTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3379-85_3379-82delinsTTAG MANE Select	ENSP00000370826.4:n.3379-85_3379-82delinsTTAG
ENST00000680789.1:c.3379-85_3379-82delinsTTAG	ENSP00000505181.1:n.3379-85_3379-82delinsTTAG
ENST00000312841.9:c.3214-85_3214-82delinsTTAG	ENSP00000326765.8:n.3214-85_3214-82delinsTTAG
ENST00000381418.8:c.3379-85_3379-82delinsTTAG	ENSP00000370826.4:n.3379-85_3379-82delinsTTAG
ENST00000522016.1:n.1572-85_1572-82delinsTTAG
NM_005144.4:c.3379-85_3379-82delinsTTAG	NP_005135.2:n.3379-85_3379-82delinsTTAG
NM_018411.4:c.3214-85_3214-82delinsTTAG	NP_060881.2:n.3214-85_3214-82delinsTTAG
XM_005273569.1:c.3382-85_3382-82delinsTTAG	XP_005273626.1:n.3382-85_3382-82delinsTTAG
XM_006716367.1:c.3217-85_3217-82delinsTTAG	XP_006716430.1:n.3217-85_3217-82delinsTTAG
XM_005273569.2:c.3382-85_3382-82delinsTTAG	XP_005273626.1:n.3382-85_3382-82delinsTTAG
XM_006716367.2:c.3217-85_3217-82delinsTTAG	XP_006716430.1:n.3217-85_3217-82delinsTTAG
NM_005144.5:c.3379-85_3379-82delinsTTAG MANE Select	NP_005135.2:n.3379-85_3379-82delinsTTAG