Canonical Allele Identifier: CA2685735641
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648506del , CM000669.2:g.152648506del GRCh38
NC_000007.13:g.152345591del , CM000669.1:g.152345591del GRCh37
NC_000007.12:g.151976524del NCBI36
NG_027988.1:g.32660del
NG_027988.2:g.32660del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*136del ENSP00000513758.1:n.*136del
ENST00000359321.2:c.*136del MANE Select ENSP00000352271.1:n.*136del
ENST00000359321.1:c.*136del ENSP00000352271.1:n.*136del
ENST00000495707.1:n.1001del
NM_005431.1:c.*136del NP_005422.1:n.*136del
NM_005431.2:c.*136del MANE Select NP_005422.1:n.*136del