Canonical Allele Identifier: CA2656969899

Gene: XRCC6

Linked Data

• gnomAD v4: 22-41635976-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41635976C>A , CM000684.2:g.41635976C>A	GRCh38
NC_000022.10:g.42031980C>A , CM000684.1:g.42031980C>A	GRCh37
NC_000022.9:g.40361926C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.8:c.196-137C>A MANE Select	ENSP00000353192.3:n.196-137C>A
ENST00000359308.8:c.196-137C>A	ENSP00000352257.4:n.196-137C>A
ENST00000360079.7:c.196-137C>A	ENSP00000353192.3:n.196-137C>A
ENST00000402580.7:c.196-260C>A	ENSP00000384941.3:n.196-260C>A
ENST00000405506.2:c.46-137C>A	ENSP00000384082.1:n.46-137C>A
ENST00000405878.5:c.196-137C>A	ENSP00000384257.1:n.196-137C>A
ENST00000428575.6:c.46-137C>A	ENSP00000403679.3:n.46-137C>A
NM_001288976.1:c.196-137C>A	NP_001275905.1:n.196-137C>A
NM_001288977.1:c.196-260C>A	NP_001275906.1:n.196-260C>A
NM_001288978.1:c.46-137C>A	NP_001275907.1:n.46-137C>A
NM_001469.4:c.196-137C>A	NP_001460.1:n.196-137C>A
NM_001288976.2:c.196-137C>A	NP_001275905.1:n.196-137C>A
NM_001288977.2:c.196-260C>A	NP_001275906.1:n.196-260C>A
NM_001469.5:c.196-137C>A MANE Select	NP_001460.1:n.196-137C>A
NM_001288978.2:c.46-137C>A	NP_001275907.1:n.46-137C>A