Canonical Allele Identifier: CA2656967716

Gene: XRCC6

Linked Data

• gnomAD v4: 22-41621319-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621319C>A , CM000684.2:g.41621319C>A	GRCh38
NC_000022.10:g.42017323C>A , CM000684.1:g.42017323C>A	GRCh37
NC_000022.9:g.40347269C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-42C>A MANE Select	ENSP00000353192.3:n.-42C>A
ENST00000360079.7:c.-42C>A	ENSP00000353192.3:n.-42C>A
ENST00000402580.7:c.-42C>A	ENSP00000384941.3:n.-42C>A
ENST00000428575.6:c.-79C>A	ENSP00000403679.3:n.-79C>A
ENST00000464116.2:n.35C>A
NM_001288977.1:c.-42C>A	NP_001275906.1:n.-42C>A
NM_001288978.1:c.-79C>A	NP_001275907.1:n.-79C>A
NM_001469.4:c.-42C>A	NP_001460.1:n.-42C>A
NM_001288976.2:c.-107C>A	NP_001275905.1:n.-107C>A
NM_001288977.2:c.-42C>A	NP_001275906.1:n.-42C>A
NM_001469.5:c.-42C>A MANE Select	NP_001460.1:n.-42C>A
NM_001288978.2:c.-79C>A	NP_001275907.1:n.-79C>A