Canonical Allele Identifier: CA2656967869

Gene: XRCC6

Linked Data

• gnomAD v4: 22-41621374-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621374T>C , CM000684.2:g.41621374T>C	GRCh38
NC_000022.10:g.42017378T>C , CM000684.1:g.42017378T>C	GRCh37
NC_000022.9:g.40347324T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-16+29T>C MANE Select	ENSP00000353192.3:n.-16+29T>C
ENST00000359308.8:c.-631T>C	ENSP00000352257.4:n.-631T>C
ENST00000360079.7:c.-16+29T>C	ENSP00000353192.3:n.-16+29T>C
ENST00000402580.7:c.-16+29T>C	ENSP00000384941.3:n.-16+29T>C
ENST00000428575.6:c.-53+29T>C	ENSP00000403679.3:n.-53+29T>C
ENST00000464116.2:n.61+29T>C
NM_001288976.1:c.-52T>C	NP_001275905.1:n.-52T>C
NM_001288977.1:c.-16+29T>C	NP_001275906.1:n.-16+29T>C
NM_001288978.1:c.-53+29T>C	NP_001275907.1:n.-53+29T>C
NM_001469.4:c.-16+29T>C	NP_001460.1:n.-16+29T>C
NM_001288976.2:c.-52T>C	NP_001275905.1:n.-52T>C
NM_001288977.2:c.-16+29T>C	NP_001275906.1:n.-16+29T>C
NM_001469.5:c.-16+29T>C MANE Select	NP_001460.1:n.-16+29T>C
NM_001288978.2:c.-53+29T>C	NP_001275907.1:n.-53+29T>C