Canonical Allele Identifier: CA345902944

Gene: RAD51AP2

Linked Data

• ClinVar Variation Id: 3151053
• ClinVar RCV Id: RCV004445442
• MyVariant Identifiers: chr2:g.17696662C>G (hg19) ; chr2:g.17515395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17515395C>G , CM000664.2:g.17515395C>G	GRCh38
NC_000002.11:g.17696662C>G , CM000664.1:g.17696662C>G	GRCh37
NC_000002.10:g.17560143C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399080.3:c.3021G>C MANE Select	ENSP00000382030.2:p.Glu1007Asp
ENST00000399080.2:c.3021G>C	ENSP00000382030.2:p.Glu1007Asp
NM_001099218.2:c.3021G>C	NP_001092688.1:p.Glu1007Asp
XM_005262625.1:c.2994G>C	XP_005262682.1:p.Glu998Asp
XM_011533084.1:c.3021G>C	XP_011531386.1:p.Glu1007Asp
NM_001321233.1:c.2994G>C	NP_001308162.1:p.Glu998Asp
XM_011533084.2:c.3021G>C	XP_011531386.1:p.Glu1007Asp
XM_024453116.1:c.2994G>C	XP_024308884.1:p.Glu998Asp
XM_024453117.1:c.2994G>C	XP_024308885.1:p.Glu998Asp
XM_024453118.1:c.2994G>C	XP_024308886.1:p.Glu998Asp
NM_001099218.3:c.3021G>C MANE Select	NP_001092688.1:p.Glu1007Asp