Canonical Allele Identifier: CA1753256996
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660567_152660569delinsCTG , CM000669.2:g.152660567_152660569delinsCTG GRCh38
NC_000007.13:g.152357652_152357654delinsCTG , CM000669.1:g.152357652_152357654delinsCTG GRCh37
NC_000007.12:g.151988585_151988587delinsCTG NCBI36
NG_027988.1:g.20597_20599delinsCAG
NG_027988.2:g.20597_20599delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11206_-47-11204delinsCAG ENSP00000513758.1:n.-47-11206_-47-11204delinsCAG
ENST00000698507.1:n.321_323delinsCAG
ENST00000359321.2:c.121+132_121+134delinsCAG MANE Select ENSP00000352271.1:n.121+132_121+134delinsCAG
ENST00000359321.1:c.121+132_121+134delinsCAG ENSP00000352271.1:n.121+132_121+134delinsCAG
ENST00000495707.1:n.143+132_143+134delinsCAG
NM_005431.1:c.121+132_121+134delinsCAG NP_005422.1:n.121+132_121+134delinsCAG
NM_005431.2:c.121+132_121+134delinsCAG MANE Select NP_005422.1:n.121+132_121+134delinsCAG