Canonical Allele Identifier: CA4582359
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs751911082
ExAC: 7:152346250 ATTTC / A
gnomAD v2: 7-152346250-ATTTC-A
gnomAD v4: 7-152649165-ATTTC-A
MyVariant Identifiers: chr7:g.152346251_152346254del (hg19) chr7:g.152649166_152649169del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649168_152649171del , CM000669.2:g.152649168_152649171del GRCh38
NC_000007.13:g.152346253_152346256del , CM000669.1:g.152346253_152346256del GRCh37
NC_000007.12:g.151977186_151977189del NCBI36
NG_027988.1:g.31997_32000del
NG_027988.2:g.31997_32000del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.148_151del ENSP00000513758.1:p.Glu50Ter
ENST00000359321.2:c.316_319del MANE Select ENSP00000352271.1:p.Glu106Ter
ENST00000359321.1:c.316_319del ENSP00000352271.1:p.Glu106Ter
ENST00000495707.1:n.338_341del
NM_005431.1:c.316_319del NP_005422.1:p.Glu106Ter
NM_005431.2:c.316_319del MANE Select NP_005422.1:p.Glu106Ter
Search 100 bp 5'
Search 100 bp 3'