Canonical Allele Identifier: CA2337560035
Community Standard Title: NM_006297.3(XRCC1):c.144+4465A=
Gene: XRCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43570445T= , CM000681.2:g.43570445T= GRCh38
NC_000019.9:g.44074597T= , CM000681.1:g.44074597T= GRCh37
NC_000019.8:g.48766437T= NCBI36
NG_033799.1:g.10134A= , LRG_784:g.10134A=

Transcript Alleles

HGVS Amino-acid Change
NM_006297.3:c.144+4465A= MANE Select NP_006288.2:n.144+4465A=
ENST00000262887.10:c.144+4465A= MANE Select ENSP00000262887.5:n.144+4465A=
NM_006297.2:c.144+4465A= , LRG_784t1:c.144+4465A= NP_006288.2:n.144+4465A=
ENST00000262887.9:c.144+4465A= ENSP00000262887.4:n.144+4465A=
ENST00000543982.5:c.51+4963A= ENSP00000443671.1:n.51+4963A=
ENST00000594107.1:c.144+4465A= ENSP00000471159.1:n.144+4465A=
ENST00000594374.1:c.170-9425A=
ENST00000595789.5:n.192+4465A=
ENST00000598165.5:c.165+4465A= ENSP00000470045.1:n.165+4465A=
ENST00000599693.5:c.71-9425A=