Canonical Allele Identifier: CA473548950

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282501T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260954T>A , CM000673.2:g.35260954T>A	GRCh38
NC_000011.9:g.35282501T>A , CM000673.1:g.35282501T>A	GRCh37
NC_000011.8:g.35239077T>A	NCBI36
NG_008727.1:g.163605A>T
NG_008727.2:g.163605A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1665A>T MANE Select	ENSP00000278379.3:p.Ala555=
ENST00000395750.6:c.1653A>T	ENSP00000379099.2:p.Ala551=
ENST00000395753.6:c.1638A>T	ENSP00000379102.1:p.Ala546=
ENST00000479543.2:n.1217A>T
ENST00000642171.1:c.*47A>T	ENSP00000495538.1:n.*47A>T
ENST00000642448.1:n.1757A>T
ENST00000642769.1:c.931A>T
ENST00000643000.1:c.1638A>T	ENSP00000495164.1:p.Ala546=
ENST00000643134.1:c.1654-2A>T	ENSP00000495188.1:n.1654-2A>T
ENST00000643522.1:c.1431A>T	ENSP00000496375.1:p.Ala477=
ENST00000644050.1:c.1638A>T	ENSP00000496123.1:p.Ala546=
ENST00000644299.1:c.1638A>T	ENSP00000494669.1:p.Ala546=
ENST00000644459.1:c.*157A>T	ENSP00000495861.1:n.*157A>T
ENST00000644779.1:c.1776A>T	ENSP00000494258.1:p.Ala592=
ENST00000644868.1:c.1727A>T	ENSP00000496760.1:n.1727A>T
ENST00000645194.1:c.1638A>T	ENSP00000496093.1:p.Ala546=
ENST00000645303.1:c.1680A>T	ENSP00000496667.1:p.Ala560=
ENST00000645542.1:n.371A>T
ENST00000645634.1:c.1638A>T	ENSP00000493945.1:p.Ala546=
ENST00000646080.1:c.1656A>T	ENSP00000494113.1:p.Ala552=
ENST00000647076.1:c.406A>T
ENST00000647104.1:c.1638A>T	ENSP00000494025.1:p.Ala546=
ENST00000278379.7:c.1665A>T	ENSP00000278379.3:p.Ala555=
ENST00000395750.5:c.1638A>T	ENSP00000379099.1:p.Ala546=
ENST00000395753.5:c.1638A>T	ENSP00000379102.1:p.Ala546=
ENST00000464522.2:c.219+4573A>T	ENSP00000435406.1:n.219+4573A>T
ENST00000479543.1:n.481A>T
NM_001195728.2:c.1638A>T	NP_001182657.1:p.Ala546=
NM_001252652.1:c.1638A>T	NP_001239581.1:p.Ala546=
NM_004171.3:c.1665A>T	NP_004162.2:p.Ala555=
XM_005253067.1:c.1656A>T	XP_005253124.1:p.Ala552=
XM_011520284.1:c.1713A>T	XP_011518586.1:p.Ala571=
XM_011520285.1:c.1653A>T	XP_011518587.1:p.Ala551=
XM_011520286.1:c.1578A>T	XP_011518588.1:p.Ala526=
XM_011520287.1:c.1479A>T	XP_011518589.1:p.Ala493=
XM_011520285.2:c.1653A>T	XP_011518587.1:p.Ala551=
XM_017018136.1:c.1680A>T	XP_016873625.1:p.Ala560=
XM_017018137.1:c.1638A>T	XP_016873626.1:p.Ala546=
XM_017018138.1:c.1638A>T	XP_016873627.1:p.Ala546=
XM_017018139.1:c.1431A>T	XP_016873628.1:p.Ala477=
NM_004171.4:c.1665A>T MANE Select	NP_004162.2:p.Ala555=
NM_001195728.3:c.1638A>T	NP_001182657.1:p.Ala546=
NM_001252652.2:c.1638A>T	NP_001239581.1:p.Ala546=