Canonical Allele Identifier: CA345902942

Gene: RAD51AP2

Linked Data

• MyVariant Identifiers: chr2:g.17696662C>A (hg19) ; chr2:g.17515395C>A (hg38)

Genomic Alleles

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

Transcript Alleles

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