Canonical Allele Identifier: CA2819043363
Gene: XRCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621318C>A , CM000684.2:g.41621318C>A GRCh38
NC_000022.10:g.42017322C>A , CM000684.1:g.42017322C>A GRCh37
NC_000022.9:g.40347268C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.8:c.-43C>A MANE Select ENSP00000353192.3:n.-43C>A
ENST00000360079.7:c.-43C>A ENSP00000353192.3:n.-43C>A
ENST00000402580.7:c.-43C>A ENSP00000384941.3:n.-43C>A
ENST00000428575.6:c.-80C>A ENSP00000403679.3:n.-80C>A
ENST00000464116.2:n.34C>A
NM_001288977.1:c.-43C>A NP_001275906.1:n.-43C>A
NM_001288978.1:c.-80C>A NP_001275907.1:n.-80C>A
NM_001469.4:c.-43C>A NP_001460.1:n.-43C>A
NM_001288976.2:c.-108C>A NP_001275905.1:n.-108C>A
NM_001288977.2:c.-43C>A NP_001275906.1:n.-43C>A
NM_001469.5:c.-43C>A MANE Select NP_001460.1:n.-43C>A
NM_001288978.2:c.-80C>A NP_001275907.1:n.-80C>A