Canonical Allele Identifier: CA2685735530
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648413_152648414insGA , CM000669.2:g.152648413_152648414insGA GRCh38
NC_000007.13:g.152345498_152345499insGA , CM000669.1:g.152345498_152345499insGA GRCh37
NC_000007.12:g.151976431_151976432insGA NCBI36
NG_027988.1:g.32752_32753insTC
NG_027988.2:g.32752_32753insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*228_*229insTC ENSP00000513758.1:n.*228_*229insTC
ENST00000359321.2:c.*228_*229insTC MANE Select ENSP00000352271.1:n.*228_*229insTC
ENST00000359321.1:c.*228_*229insTC ENSP00000352271.1:n.*228_*229insTC
ENST00000495707.1:n.1093_1094insTC
NM_005431.1:c.*228_*229insTC NP_005422.1:n.*228_*229insTC
NM_005431.2:c.*228_*229insTC MANE Select NP_005422.1:n.*228_*229insTC