Canonical Allele Identifier: CA1538811
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2355111
ClinVar RCV Id: RCV004190565
dbSNP Id: rs200764188
gnomAD v2: 2-17697089-A-G
gnomAD v3: 2-17515822-A-G
gnomAD v4: 2-17515822-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17515822A>G , CM000664.2:g.17515822A>G GRCh38
NC_000002.11:g.17697089A>G , CM000664.1:g.17697089A>G GRCh37
NC_000002.10:g.17560570A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000399080.3:c.2594T>C MANE Select ENSP00000382030.2:p.Phe865Ser
ENST00000399080.2:c.2594T>C ENSP00000382030.2:p.Phe865Ser
NM_001099218.2:c.2594T>C NP_001092688.1:p.Phe865Ser
XM_005262625.1:c.2567T>C XP_005262682.1:p.Phe856Ser
XM_011533084.1:c.2594T>C XP_011531386.1:p.Phe865Ser
NM_001321233.1:c.2567T>C NP_001308162.1:p.Phe856Ser
XM_011533084.2:c.2594T>C XP_011531386.1:p.Phe865Ser
XM_024453116.1:c.2567T>C XP_024308884.1:p.Phe856Ser
XM_024453117.1:c.2567T>C XP_024308885.1:p.Phe856Ser
XM_024453118.1:c.2567T>C XP_024308886.1:p.Phe856Ser
NM_001099218.3:c.2594T>C MANE Select NP_001092688.1:p.Phe865Ser