Canonical Allele Identifier: CA2406336656

Gene: XRCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621366T= , CM000684.2:g.41621366T=	GRCh38
NC_000022.10:g.42017370T= , CM000684.1:g.42017370T=	GRCh37
NC_000022.9:g.40347316T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-16+21T= MANE Select	ENSP00000353192.3:n.-16+21T=
ENST00000359308.8:c.-639T=	ENSP00000352257.4:n.-639T=
ENST00000360079.7:c.-16+21T=	ENSP00000353192.3:n.-16+21T=
ENST00000402580.7:c.-16+21T=	ENSP00000384941.3:n.-16+21T=
ENST00000428575.6:c.-53+21T=	ENSP00000403679.3:n.-53+21T=
ENST00000464116.2:n.61+21T=
NM_001288976.1:c.-60T=	NP_001275905.1:n.-60T=
NM_001288977.1:c.-16+21T=	NP_001275906.1:n.-16+21T=
NM_001288978.1:c.-53+21T=	NP_001275907.1:n.-53+21T=
NM_001469.4:c.-16+21T=	NP_001460.1:n.-16+21T=
NM_001288976.2:c.-60T=	NP_001275905.1:n.-60T=
NM_001288977.2:c.-16+21T=	NP_001275906.1:n.-16+21T=
NM_001469.5:c.-16+21T= MANE Select	NP_001460.1:n.-16+21T=
NM_001288978.2:c.-53+21T=	NP_001275907.1:n.-53+21T=