Canonical Allele Identifier: CA2656967766
Gene: XRCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621338C>A , CM000684.2:g.41621338C>A GRCh38
NC_000022.10:g.42017342C>A , CM000684.1:g.42017342C>A GRCh37
NC_000022.9:g.40347288C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.8:c.-23C>A MANE Select ENSP00000353192.3:n.-23C>A
ENST00000360079.7:c.-23C>A ENSP00000353192.3:n.-23C>A
ENST00000402580.7:c.-23C>A ENSP00000384941.3:n.-23C>A
ENST00000428575.6:c.-60C>A ENSP00000403679.3:n.-60C>A
ENST00000464116.2:n.54C>A
NM_001288977.1:c.-23C>A NP_001275906.1:n.-23C>A
NM_001288978.1:c.-60C>A NP_001275907.1:n.-60C>A
NM_001469.4:c.-23C>A NP_001460.1:n.-23C>A
NM_001288976.2:c.-88C>A NP_001275905.1:n.-88C>A
NM_001288977.2:c.-23C>A NP_001275906.1:n.-23C>A
NM_001469.5:c.-23C>A MANE Select NP_001460.1:n.-23C>A
NM_001288978.2:c.-60C>A NP_001275907.1:n.-60C>A