Canonical Allele Identifier: CA2337551431
Gene: XRCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1972579532

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43551897_43551898insT , CM000681.2:g.43551897_43551898insT GRCh38
NC_000019.9:g.44056049_44056050insT , CM000681.1:g.44056049_44056050insT GRCh37
NC_000019.8:g.48747889_48747890insT NCBI36
NG_033799.1:g.28681_28682insA , LRG_784:g.28681_28682insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262887.10:c.1082+119_1082+120insA MANE Select ENSP00000262887.5:n.1082+119_1082+120insA
ENST00000262887.9:c.1082+119_1082+120insA ENSP00000262887.4:n.1082+119_1082+120insA
ENST00000543982.5:c.989+119_989+120insA ENSP00000443671.1:n.989+119_989+120insA
ENST00000597811.5:c.692+119_692+120insA
NM_006297.2:c.1082+119_1082+120insA , LRG_784t1:c.1082+119_1082+120insA NP_006288.2:n.1082+119_1082+120insA
NM_006297.3:c.1082+119_1082+120insA MANE Select NP_006288.2:n.1082+119_1082+120insA