Canonical Allele Identifier: CA1770254743

Gene: HR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116503_22116509delinsGCTTCCT , CM000670.2:g.22116503_22116509delinsGCTTCCT	GRCh38
NC_000008.10:g.21974016_21974022delinsGCTTCCT , CM000670.1:g.21974016_21974022delinsGCTTCCT	GRCh37
NC_000008.9:g.22029961_22029967delinsGCTTCCT	NCBI36
NG_008166.1:g.19009_19015delinsAGGAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3379-81_3379-75delinsAGGAAGC MANE Select	ENSP00000370826.4:n.3379-81_3379-75delinsAGGAAGC
ENST00000680789.1:c.3379-81_3379-75delinsAGGAAGC	ENSP00000505181.1:n.3379-81_3379-75delinsAGGAAGC
ENST00000312841.9:c.3214-81_3214-75delinsAGGAAGC	ENSP00000326765.8:n.3214-81_3214-75delinsAGGAAGC
ENST00000381418.8:c.3379-81_3379-75delinsAGGAAGC	ENSP00000370826.4:n.3379-81_3379-75delinsAGGAAGC
ENST00000522016.1:n.1572-81_1572-75delinsAGGAAGC
NM_005144.4:c.3379-81_3379-75delinsAGGAAGC	NP_005135.2:n.3379-81_3379-75delinsAGGAAGC
NM_018411.4:c.3214-81_3214-75delinsAGGAAGC	NP_060881.2:n.3214-81_3214-75delinsAGGAAGC
XM_005273569.1:c.3382-81_3382-75delinsAGGAAGC	XP_005273626.1:n.3382-81_3382-75delinsAGGAAGC
XM_006716367.1:c.3217-81_3217-75delinsAGGAAGC	XP_006716430.1:n.3217-81_3217-75delinsAGGAAGC
XM_005273569.2:c.3382-81_3382-75delinsAGGAAGC	XP_005273626.1:n.3382-81_3382-75delinsAGGAAGC
XM_006716367.2:c.3217-81_3217-75delinsAGGAAGC	XP_006716430.1:n.3217-81_3217-75delinsAGGAAGC
NM_005144.5:c.3379-81_3379-75delinsAGGAAGC MANE Select	NP_005135.2:n.3379-81_3379-75delinsAGGAAGC