Canonical Allele Identifier: CA2406336605
Gene: XRCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621316G= , CM000684.2:g.41621316G= GRCh38
NC_000022.10:g.42017320G= , CM000684.1:g.42017320G= GRCh37
NC_000022.9:g.40347266G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.8:c.-45G= MANE Select ENSP00000353192.3:n.-45G=
ENST00000360079.7:c.-45G= ENSP00000353192.3:n.-45G=
ENST00000402580.7:c.-45G= ENSP00000384941.3:n.-45G=
ENST00000428575.6:c.-82G= ENSP00000403679.3:n.-82G=
ENST00000464116.2:n.32G=
NM_001288977.1:c.-45G= NP_001275906.1:n.-45G=
NM_001288978.1:c.-82G= NP_001275907.1:n.-82G=
NM_001469.4:c.-45G= NP_001460.1:n.-45G=
NM_001288976.2:c.-110G= NP_001275905.1:n.-110G=
NM_001288977.2:c.-45G= NP_001275906.1:n.-45G=
NM_001469.5:c.-45G= MANE Select NP_001460.1:n.-45G=
NM_001288978.2:c.-82G= NP_001275907.1:n.-82G=