Canonical Allele Identifier: CA2406336593
Gene: XRCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621305T= , CM000684.2:g.41621305T= GRCh38
NC_000022.10:g.42017309T= , CM000684.1:g.42017309T= GRCh37
NC_000022.9:g.40347255T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.8:c.-56T= MANE Select ENSP00000353192.3:n.-56T=
ENST00000360079.7:c.-56T= ENSP00000353192.3:n.-56T=
ENST00000402580.7:c.-56T= ENSP00000384941.3:n.-56T=
ENST00000428575.6:c.-93T= ENSP00000403679.3:n.-93T=
ENST00000464116.2:n.21T=
NM_001288977.1:c.-56T= NP_001275906.1:n.-56T=
NM_001288978.1:c.-93T= NP_001275907.1:n.-93T=
NM_001469.4:c.-56T= NP_001460.1:n.-56T=
NM_001288976.2:c.-121T= NP_001275905.1:n.-121T=
NM_001288977.2:c.-56T= NP_001275906.1:n.-56T=
NM_001469.5:c.-56T= MANE Select NP_001460.1:n.-56T=
NM_001288978.2:c.-93T= NP_001275907.1:n.-93T=