Canonical Allele Identifier: CA1518599

Gene: RSAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.6890255A>G , CM000664.2:g.6890255A>G	GRCh38
NC_000002.11:g.7030386A>G , CM000664.1:g.7030386A>G	GRCh37
NC_000002.10:g.6947837A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382040.4:c.818A>G MANE Select	ENSP00000371471.3:p.Asp273Gly
ENST00000442639.6:c.614A>G	ENSP00000406427.2:p.Asp205Gly
ENST00000679373.1:c.*617A>G	ENSP00000505885.1:n.*617A>G
ENST00000679863.1:c.*1862A>G	ENSP00000505443.1:n.*1862A>G
ENST00000680320.1:c.452A>G	ENSP00000505832.1:p.Asp151Gly
ENST00000680607.1:c.818A>G	ENSP00000506390.1:p.Asp273Gly
ENST00000382040.3:c.818A>G	ENSP00000371471.3:p.Asp273Gly
NM_080657.4:c.818A>G	NP_542388.2:p.Asp273Gly
XM_011510414.1:c.818A>G	XP_011508716.1:p.Asp273Gly
XM_011510415.1:c.614A>G	XP_011508717.1:p.Asp205Gly
XM_011510415.2:c.614A>G	XP_011508717.1:p.Asp205Gly
NM_080657.5:c.818A>G MANE Select	NP_542388.2:p.Asp273Gly