Canonical Allele Identifier: CA2406345136

Gene: XRCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41635851T= , CM000684.2:g.41635851T=	GRCh38
NC_000022.10:g.42031855T= , CM000684.1:g.42031855T=	GRCh37
NC_000022.9:g.40361801T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.8:c.196-262T= MANE Select	ENSP00000353192.3:n.196-262T=
ENST00000359308.8:c.196-262T=	ENSP00000352257.4:n.196-262T=
ENST00000360079.7:c.196-262T=	ENSP00000353192.3:n.196-262T=
ENST00000402580.7:c.196-385T=	ENSP00000384941.3:n.196-385T=
ENST00000405506.2:c.46-262T=	ENSP00000384082.1:n.46-262T=
ENST00000405878.5:c.196-262T=	ENSP00000384257.1:n.196-262T=
ENST00000428575.6:c.46-262T=	ENSP00000403679.3:n.46-262T=
NM_001288976.1:c.196-262T=	NP_001275905.1:n.196-262T=
NM_001288977.1:c.196-385T=	NP_001275906.1:n.196-385T=
NM_001288978.1:c.46-262T=	NP_001275907.1:n.46-262T=
NM_001469.4:c.196-262T=	NP_001460.1:n.196-262T=
NM_001288976.2:c.196-262T=	NP_001275905.1:n.196-262T=
NM_001288977.2:c.196-385T=	NP_001275906.1:n.196-385T=
NM_001469.5:c.196-262T= MANE Select	NP_001460.1:n.196-262T=
NM_001288978.2:c.46-262T=	NP_001275907.1:n.46-262T=