Canonical Allele Identifier: CA2685735727
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648600_152648602del , CM000669.2:g.152648600_152648602del GRCh38
NC_000007.13:g.152345685_152345687del , CM000669.1:g.152345685_152345687del GRCh37
NC_000007.12:g.151976618_151976620del NCBI36
NG_027988.1:g.32564_32566del
NG_027988.2:g.32564_32566del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*40_*42del ENSP00000513758.1:n.*40_*42del
ENST00000359321.2:c.*40_*42del MANE Select ENSP00000352271.1:n.*40_*42del
ENST00000359321.1:c.*40_*42del ENSP00000352271.1:n.*40_*42del
ENST00000495707.1:n.905_907del
NM_005431.1:c.*40_*42del NP_005422.1:n.*40_*42del
NM_005431.2:c.*40_*42del MANE Select NP_005422.1:n.*40_*42del