Canonical Allele Identifier: CA633476304
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1171529602
gnomAD v2: 19-44055858-GA-G
gnomAD v3: 19-43551706-GA-G
gnomAD v4: 19-43551706-GA-G
MyVariant Identifiers: chr19:g.44055859del (hg19) chr19:g.43551707del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551708del , CM000681.2:g.43551708del GRCh38
NC_000019.9:g.44055860del , CM000681.1:g.44055860del GRCh37
NC_000019.8:g.48747700del NCBI36
NG_033799.1:g.28872del , LRG_784:g.28872del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1083-20del MANE Select ENSP00000262887.5:n.1083-20del
ENST00000262887.9:c.1083-20del ENSP00000262887.4:n.1083-20del
ENST00000543982.5:c.990-20del ENSP00000443671.1:n.990-20del
ENST00000597811.5:c.693-20del
NM_006297.2:c.1083-20del , LRG_784t1:c.1083-20del NP_006288.2:n.1083-20del
NM_006297.3:c.1083-20del MANE Select NP_006288.2:n.1083-20del
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