Canonical Allele Identifier: CA345916182

Gene: RAD51AP2

Linked Data

• ClinVar Variation Id: 2481609
• ClinVar RCV Id: RCV004266105
• MyVariant Identifiers: chr2:g.17698653C>T (hg19) ; chr2:g.17517386C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17517386C>T , CM000664.2:g.17517386C>T	GRCh38
NC_000002.11:g.17698653C>T , CM000664.1:g.17698653C>T	GRCh37
NC_000002.10:g.17562134C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399080.3:c.1030G>A MANE Select	ENSP00000382030.2:p.Asp344Asn
ENST00000399080.2:c.1030G>A	ENSP00000382030.2:p.Asp344Asn
NM_001099218.2:c.1030G>A	NP_001092688.1:p.Asp344Asn
XM_005262625.1:c.1003G>A	XP_005262682.1:p.Asp335Asn
XM_011533084.1:c.1030G>A	XP_011531386.1:p.Asp344Asn
NM_001321233.1:c.1003G>A	NP_001308162.1:p.Asp335Asn
XM_011533084.2:c.1030G>A	XP_011531386.1:p.Asp344Asn
XM_024453116.1:c.1003G>A	XP_024308884.1:p.Asp335Asn
XM_024453117.1:c.1003G>A	XP_024308885.1:p.Asp335Asn
XM_024453118.1:c.1003G>A	XP_024308886.1:p.Asp335Asn
NM_001099218.3:c.1030G>A MANE Select	NP_001092688.1:p.Asp344Asn