Canonical Allele Identifier: CA2406336664
Gene: XRCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621381G= , CM000684.2:g.41621381G= GRCh38
NC_000022.10:g.42017385G= , CM000684.1:g.42017385G= GRCh37
NC_000022.9:g.40347331G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.8:c.-16+36G= MANE Select ENSP00000353192.3:n.-16+36G=
ENST00000359308.8:c.-624G= ENSP00000352257.4:n.-624G=
ENST00000360079.7:c.-16+36G= ENSP00000353192.3:n.-16+36G=
ENST00000402580.7:c.-16+36G= ENSP00000384941.3:n.-16+36G=
ENST00000428575.6:c.-53+36G= ENSP00000403679.3:n.-53+36G=
ENST00000464116.2:n.61+36G=
NM_001288976.1:c.-45G= NP_001275905.1:n.-45G=
NM_001288977.1:c.-16+36G= NP_001275906.1:n.-16+36G=
NM_001288978.1:c.-53+36G= NP_001275907.1:n.-53+36G=
NM_001469.4:c.-16+36G= NP_001460.1:n.-16+36G=
NM_001288976.2:c.-45G= NP_001275905.1:n.-45G=
NM_001288977.2:c.-16+36G= NP_001275906.1:n.-16+36G=
NM_001469.5:c.-16+36G= MANE Select NP_001460.1:n.-16+36G=
NM_001288978.2:c.-53+36G= NP_001275907.1:n.-53+36G=