Canonical Allele Identifier: CA2656967762

Gene: XRCC6

Linked Data

• gnomAD v4: 22-41621336-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621336T>G , CM000684.2:g.41621336T>G	GRCh38
NC_000022.10:g.42017340T>G , CM000684.1:g.42017340T>G	GRCh37
NC_000022.9:g.40347286T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-25T>G MANE Select	ENSP00000353192.3:n.-25T>G
ENST00000360079.7:c.-25T>G	ENSP00000353192.3:n.-25T>G
ENST00000402580.7:c.-25T>G	ENSP00000384941.3:n.-25T>G
ENST00000428575.6:c.-62T>G	ENSP00000403679.3:n.-62T>G
ENST00000464116.2:n.52T>G
NM_001288977.1:c.-25T>G	NP_001275906.1:n.-25T>G
NM_001288978.1:c.-62T>G	NP_001275907.1:n.-62T>G
NM_001469.4:c.-25T>G	NP_001460.1:n.-25T>G
NM_001288976.2:c.-90T>G	NP_001275905.1:n.-90T>G
NM_001288977.2:c.-25T>G	NP_001275906.1:n.-25T>G
NM_001469.5:c.-25T>G MANE Select	NP_001460.1:n.-25T>G
NM_001288978.2:c.-62T>G	NP_001275907.1:n.-62T>G