Canonical Allele Identifier: CA1963609591

Gene: SLC1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35259305A= , CM000673.2:g.35259305A=	GRCh38
NC_000011.9:g.35280852A= , CM000673.1:g.35280852A=	GRCh37
NC_000011.8:g.35237428A=	NCBI36
NG_008727.1:g.165254T=
NG_008727.2:g.165254T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004171.4:c.*1589T= MANE Select	NP_004162.2:n.*1589T=
ENST00000278379.9:c.*1589T= MANE Select	ENSP00000278379.3:n.*1589T=
NM_001195728.2:c.*1589T=	NP_001182657.1:n.*1589T=
NM_001195728.3:c.*1589T=	NP_001182657.1:n.*1589T=
NM_001252652.1:c.*1589T=	NP_001239581.1:n.*1589T=
NM_001252652.2:c.*1589T=	NP_001239581.1:n.*1589T=
NM_004171.3:c.*1589T=	NP_004162.2:n.*1589T=
ENST00000278379.7:c.*1589T=	ENSP00000278379.3:n.*1589T=
ENST00000395750.5:c.*1589T=	ENSP00000379099.1:n.*1589T=
ENST00000395750.6:c.*1589T=	ENSP00000379099.2:n.*1589T=
ENST00000395753.5:c.*1589T=	ENSP00000379102.1:n.*1589T=
ENST00000395753.6:c.*1589T=	ENSP00000379102.1:n.*1589T=
ENST00000464522.2:c.220-4497T=	ENSP00000435406.1:n.220-4497T=
ENST00000479543.2:n.2866T=
ENST00000642171.1:c.*1696T=	ENSP00000495538.1:n.*1696T=
ENST00000642769.1:c.1041+1539T=
ENST00000643522.1:c.*1589T=	ENSP00000496375.1:n.*1589T=
ENST00000644050.1:c.*1589T=	ENSP00000496123.1:n.*1589T=
ENST00000644459.1:c.*1806T=	ENSP00000495861.1:n.*1806T=
ENST00000644779.1:c.*1589T=	ENSP00000494258.1:n.*1589T=
ENST00000645303.1:c.*1589T=	ENSP00000496667.1:n.*1589T=
ENST00000647076.1:c.516+1539T=
XM_005253067.1:c.*1589T=	XP_005253124.1:n.*1589T=
XM_011520284.1:c.*1589T=	XP_011518586.1:n.*1589T=
XM_011520285.1:c.*1589T=	XP_011518587.1:n.*1589T=
XM_011520285.2:c.*1589T=	XP_011518587.1:n.*1589T=
XM_011520286.1:c.*1589T=	XP_011518588.1:n.*1589T=
XM_011520287.1:c.*1589T=	XP_011518589.1:n.*1589T=
XM_017018136.1:c.*1589T=	XP_016873625.1:n.*1589T=
XM_017018137.1:c.*1589T=	XP_016873626.1:n.*1589T=
XM_017018138.1:c.*1589T=	XP_016873627.1:n.*1589T=
XM_017018139.1:c.*1589T=	XP_016873628.1:n.*1589T=