Canonical Allele Identifier: CA3518983

Gene: SLC36A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151344186C>T , CM000667.2:g.151344186C>T	GRCh38
NC_000005.9:g.150723747C>T , CM000667.1:g.150723747C>T	GRCh37
NC_000005.8:g.150703940C>T	NCBI36
NG_027745.1:g.8405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335244.9:c.246G>A MANE Select	ENSP00000334223.4:p.Ala82=
ENST00000335244.8:c.246G>A	ENSP00000334223.4:p.Ala82=
ENST00000518280.5:c.246G>A	ENSP00000428453.1:p.Ala82=
ENST00000518617.5:c.246G>A	ENSP00000430149.1:p.Ala82=
ENST00000521967.1:c.246G>A	ENSP00000430535.1:p.Ala82=
ENST00000522829.1:n.342G>A
NM_181776.2:c.246G>A	NP_861441.2:p.Ala82=
XM_005268377.3:c.246G>A	XP_005268434.1:p.Ala82=
XM_006714756.2:c.246G>A	XP_006714819.1:p.Ala82=
XM_011537559.1:c.246G>A	XP_011535861.1:p.Ala82=
XM_005268377.4:c.246G>A	XP_005268434.1:p.Ala82=
XM_006714756.4:c.246G>A	XP_006714819.1:p.Ala82=
XM_017009083.2:c.246G>A	XP_016864572.1:p.Ala82=
XM_017009084.1:c.-264G>A	XP_016864573.1:n.-264G>A
NM_181776.3:c.246G>A MANE Select	NP_861441.2:p.Ala82=