Canonical Allele Identifier: CA369571979

Gene: OR9A4 MGAM

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141919663A>G , CM000669.2:g.141919663A>G	GRCh38
NC_000007.13:g.141619463A>G , CM000669.1:g.141619463A>G	GRCh37
NC_000007.12:g.141265932A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001001656.3:c.788A>G (OR9A4) MANE Select	NP_001001656.1:p.Lys263Arg
ENST00000641559.1:c.788A>G (OR9A4) MANE Select	ENSP00000493151.1:p.Lys263Arg
NM_001001656.1:c.788A>G (OR9A4)	NP_001001656.1:p.Lys263Arg
NM_001001656.2:c.788A>G (OR9A4)	NP_001001656.1:p.Lys263Arg
ENST00000465654.5:c.-180+11795A>G (MGAM)	ENSP00000419372.1:n.-180+11795A>G
ENST00000497554.1:n.37-10114A>G (MGAM)
ENST00000548136.1:c.788A>G (OR9A4)	ENSP00000448789.1:p.Lys263Arg
XM_011515783.1:c.788A>G (OR9A4)	XP_011514085.1:p.Lys263Arg
XM_011515784.1:c.788A>G (OR9A4)	XP_011514086.1:p.Lys263Arg