Canonical Allele Identifier: CA2656967695

Gene: XRCC6

Linked Data

• gnomAD v4: 22-41621310-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621310T>C , CM000684.2:g.41621310T>C	GRCh38
NC_000022.10:g.42017314T>C , CM000684.1:g.42017314T>C	GRCh37
NC_000022.9:g.40347260T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-51T>C MANE Select	ENSP00000353192.3:n.-51T>C
ENST00000360079.7:c.-51T>C	ENSP00000353192.3:n.-51T>C
ENST00000402580.7:c.-51T>C	ENSP00000384941.3:n.-51T>C
ENST00000428575.6:c.-88T>C	ENSP00000403679.3:n.-88T>C
ENST00000464116.2:n.26T>C
NM_001288977.1:c.-51T>C	NP_001275906.1:n.-51T>C
NM_001288978.1:c.-88T>C	NP_001275907.1:n.-88T>C
NM_001469.4:c.-51T>C	NP_001460.1:n.-51T>C
NM_001288976.2:c.-116T>C	NP_001275905.1:n.-116T>C
NM_001288977.2:c.-51T>C	NP_001275906.1:n.-51T>C
NM_001469.5:c.-51T>C MANE Select	NP_001460.1:n.-51T>C
NM_001288978.2:c.-88T>C	NP_001275907.1:n.-88T>C