Canonical Allele Identifier: CA345916122

Gene: RAD51AP2

Linked Data

• MyVariant Identifiers: chr2:g.17698642A>C (hg19) ; chr2:g.17517375A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17517375A>C , CM000664.2:g.17517375A>C	GRCh38
NC_000002.11:g.17698642A>C , CM000664.1:g.17698642A>C	GRCh37
NC_000002.10:g.17562123A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399080.3:c.1041T>G MANE Select	ENSP00000382030.2:p.Ser347Arg
ENST00000399080.2:c.1041T>G	ENSP00000382030.2:p.Ser347Arg
NM_001099218.2:c.1041T>G	NP_001092688.1:p.Ser347Arg
XM_005262625.1:c.1014T>G	XP_005262682.1:p.Ser338Arg
XM_011533084.1:c.1041T>G	XP_011531386.1:p.Ser347Arg
NM_001321233.1:c.1014T>G	NP_001308162.1:p.Ser338Arg
XM_011533084.2:c.1041T>G	XP_011531386.1:p.Ser347Arg
XM_024453116.1:c.1014T>G	XP_024308884.1:p.Ser338Arg
XM_024453117.1:c.1014T>G	XP_024308885.1:p.Ser338Arg
XM_024453118.1:c.1014T>G	XP_024308886.1:p.Ser338Arg
NM_001099218.3:c.1041T>G MANE Select	NP_001092688.1:p.Ser347Arg