Canonical Allele Identifier: CA2406336647

Gene: XRCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621357G= , CM000684.2:g.41621357G=	GRCh38
NC_000022.10:g.42017361G= , CM000684.1:g.42017361G=	GRCh37
NC_000022.9:g.40347307G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-16+12G= MANE Select	ENSP00000353192.3:n.-16+12G=
ENST00000359308.8:c.-648G=	ENSP00000352257.4:n.-648G=
ENST00000360079.7:c.-16+12G=	ENSP00000353192.3:n.-16+12G=
ENST00000402580.7:c.-16+12G=	ENSP00000384941.3:n.-16+12G=
ENST00000428575.6:c.-53+12G=	ENSP00000403679.3:n.-53+12G=
ENST00000464116.2:n.61+12G=
NM_001288976.1:c.-69G=	NP_001275905.1:n.-69G=
NM_001288977.1:c.-16+12G=	NP_001275906.1:n.-16+12G=
NM_001288978.1:c.-53+12G=	NP_001275907.1:n.-53+12G=
NM_001469.4:c.-16+12G=	NP_001460.1:n.-16+12G=
NM_001288976.2:c.-69G=	NP_001275905.1:n.-69G=
NM_001288977.2:c.-16+12G=	NP_001275906.1:n.-16+12G=
NM_001469.5:c.-16+12G= MANE Select	NP_001460.1:n.-16+12G=
NM_001288978.2:c.-53+12G=	NP_001275907.1:n.-53+12G=