Canonical Allele Identifier: CA753224972

Gene: XRCC6

Linked Data

• dbSNP Id: rs1324927026
• gnomAD v3: 22-41635892-T-TA
• gnomAD v4: 22-41635892-T-TA
• MyVariant Identifiers: chr22:g.42031896_42031897insA (hg19) ; chr22:g.41635892_41635893insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41635893dup , CM000684.2:g.41635893dup	GRCh38
NC_000022.10:g.42031897dup , CM000684.1:g.42031897dup	GRCh37
NC_000022.9:g.40361843dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.196-220dup MANE Select	ENSP00000353192.3:n.196-220dup
ENST00000359308.8:c.196-220dup	ENSP00000352257.4:n.196-220dup
ENST00000360079.7:c.196-220dup	ENSP00000353192.3:n.196-220dup
ENST00000402580.7:c.196-343dup	ENSP00000384941.3:n.196-343dup
ENST00000405506.2:c.46-220dup	ENSP00000384082.1:n.46-220dup
ENST00000405878.5:c.196-220dup	ENSP00000384257.1:n.196-220dup
ENST00000428575.6:c.46-220dup	ENSP00000403679.3:n.46-220dup
NM_001288976.1:c.196-220dup	NP_001275905.1:n.196-220dup
NM_001288977.1:c.196-343dup	NP_001275906.1:n.196-343dup
NM_001288978.1:c.46-220dup	NP_001275907.1:n.46-220dup
NM_001469.4:c.196-220dup	NP_001460.1:n.196-220dup
NM_001288976.2:c.196-220dup	NP_001275905.1:n.196-220dup
NM_001288977.2:c.196-343dup	NP_001275906.1:n.196-343dup
NM_001469.5:c.196-220dup MANE Select	NP_001460.1:n.196-220dup
NM_001288978.2:c.46-220dup	NP_001275907.1:n.46-220dup