Canonical Allele Identifier: CA406205523

Gene: XRCC1

Linked Data

• MyVariant Identifiers: chr19:g.44056416T>G (hg19) ; chr19:g.43552264T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43552264T>G , CM000681.2:g.43552264T>G	GRCh38
NC_000019.9:g.44056416T>G , CM000681.1:g.44056416T>G	GRCh37
NC_000019.8:g.48748256T>G	NCBI36
NG_033799.1:g.28315A>C , LRG_784:g.28315A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262887.10:c.835A>C MANE Select	ENSP00000262887.5:p.Thr279Pro
ENST00000262887.9:c.835A>C	ENSP00000262887.4:p.Thr279Pro
ENST00000543982.5:c.742A>C	ENSP00000443671.1:p.Thr248Pro
ENST00000595789.5:n.956A>C
ENST00000597811.5:c.445A>C
ENST00000598165.5:c.856A>C	ENSP00000470045.1:p.Thr286Pro
ENST00000598422.1:n.515A>C
NM_006297.2:c.835A>C , LRG_784t1:c.835A>C	NP_006288.2:p.Thr279Pro
NM_006297.3:c.835A>C MANE Select	NP_006288.2:p.Thr279Pro