Canonical Allele Identifier: CA2686428458

Gene: HR

Linked Data

• gnomAD v4: 8-22116271-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22116271C>A , CM000670.2:g.22116271C>A	GRCh38
NC_000008.10:g.21973784C>A , CM000670.1:g.21973784C>A	GRCh37
NC_000008.9:g.22029729C>A	NCBI36
NG_008166.1:g.19247G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381418.9:c.3507+29G>T MANE Select	ENSP00000370826.4:n.3507+29G>T
ENST00000680789.1:c.3507+29G>T	ENSP00000505181.1:n.3507+29G>T
ENST00000312841.9:c.3342+29G>T	ENSP00000326765.8:n.3342+29G>T
ENST00000381418.8:c.3507+29G>T	ENSP00000370826.4:n.3507+29G>T
ENST00000522016.1:n.1700+29G>T
NM_005144.4:c.3507+29G>T	NP_005135.2:n.3507+29G>T
NM_018411.4:c.3342+29G>T	NP_060881.2:n.3342+29G>T
XM_005273569.1:c.3510+29G>T	XP_005273626.1:n.3510+29G>T
XM_006716367.1:c.3345+29G>T	XP_006716430.1:n.3345+29G>T
XM_005273569.2:c.3510+29G>T	XP_005273626.1:n.3510+29G>T
XM_006716367.2:c.3345+29G>T	XP_006716430.1:n.3345+29G>T
NM_005144.5:c.3507+29G>T MANE Select	NP_005135.2:n.3507+29G>T