Canonical Allele Identifier: CA2819043362

Gene: XRCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621312T>G , CM000684.2:g.41621312T>G	GRCh38
NC_000022.10:g.42017316T>G , CM000684.1:g.42017316T>G	GRCh37
NC_000022.9:g.40347262T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-49T>G MANE Select	ENSP00000353192.3:n.-49T>G
ENST00000360079.7:c.-49T>G	ENSP00000353192.3:n.-49T>G
ENST00000402580.7:c.-49T>G	ENSP00000384941.3:n.-49T>G
ENST00000428575.6:c.-86T>G	ENSP00000403679.3:n.-86T>G
ENST00000464116.2:n.28T>G
NM_001288977.1:c.-49T>G	NP_001275906.1:n.-49T>G
NM_001288978.1:c.-86T>G	NP_001275907.1:n.-86T>G
NM_001469.4:c.-49T>G	NP_001460.1:n.-49T>G
NM_001288976.2:c.-114T>G	NP_001275905.1:n.-114T>G
NM_001288977.2:c.-49T>G	NP_001275906.1:n.-49T>G
NM_001469.5:c.-49T>G MANE Select	NP_001460.1:n.-49T>G
NM_001288978.2:c.-86T>G	NP_001275907.1:n.-86T>G