Canonical Allele Identifier: CA2685735539
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648427_152648428insGAA , CM000669.2:g.152648427_152648428insGAA GRCh38
NC_000007.13:g.152345512_152345513insGAA , CM000669.1:g.152345512_152345513insGAA GRCh37
NC_000007.12:g.151976445_151976446insGAA NCBI36
NG_027988.1:g.32740_32741insCTT
NG_027988.2:g.32740_32741insCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*216_*217insCTT ENSP00000513758.1:n.*216_*217insCTT
ENST00000359321.2:c.*216_*217insCTT MANE Select ENSP00000352271.1:n.*216_*217insCTT
ENST00000359321.1:c.*216_*217insCTT ENSP00000352271.1:n.*216_*217insCTT
ENST00000495707.1:n.1081_1082insCTT
NM_005431.1:c.*216_*217insCTT NP_005422.1:n.*216_*217insCTT
NM_005431.2:c.*216_*217insCTT MANE Select NP_005422.1:n.*216_*217insCTT