Canonical Allele Identifier: CA473545919

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35308402A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35286855A>G , CM000673.2:g.35286855A>G	GRCh38
NC_000011.9:g.35308402A>G , CM000673.1:g.35308402A>G	GRCh37
NC_000011.8:g.35264978A>G	NCBI36
NG_008727.1:g.137704T>C
NG_008727.2:g.137704T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1188T>C MANE Select	ENSP00000278379.3:p.Ile396=
ENST00000395750.6:c.1176T>C	ENSP00000379099.2:p.Ile392=
ENST00000395753.6:c.1161T>C	ENSP00000379102.1:p.Ile387=
ENST00000449068.2:c.1188T>C	ENSP00000406133.2:p.Ile396=
ENST00000479543.2:n.740T>C
ENST00000531628.2:c.1188T>C	ENSP00000436029.2:p.Ile396=
ENST00000606205.6:c.1188T>C	ENSP00000476124.2:p.Ile396=
ENST00000642171.1:c.1188T>C	ENSP00000495538.1:p.Ile396=
ENST00000642183.1:n.1216T>C
ENST00000642216.1:n.736T>C
ENST00000642224.1:n.1350T>C
ENST00000642448.1:n.1280T>C
ENST00000642578.1:c.1161T>C	ENSP00000494076.1:p.Ile387=
ENST00000642769.1:c.454T>C
ENST00000643000.1:c.1161T>C	ENSP00000495164.1:p.Ile387=
ENST00000643134.1:c.1188T>C	ENSP00000495188.1:p.Ile396=
ENST00000643305.1:c.1188T>C	ENSP00000494828.1:p.Ile396=
ENST00000643454.1:c.1179T>C	ENSP00000495126.1:p.Ile393=
ENST00000643522.1:c.954T>C	ENSP00000496375.1:p.Ile318=
ENST00000644050.1:c.1161T>C	ENSP00000496123.1:p.Ile387=
ENST00000644299.1:c.1161T>C	ENSP00000494669.1:p.Ile387=
ENST00000644351.1:c.1188T>C	ENSP00000496587.1:p.Ile396=
ENST00000644459.1:c.1188T>C	ENSP00000495861.1:p.Ile396=
ENST00000644779.1:c.1299T>C	ENSP00000494258.1:p.Ile433=
ENST00000644868.1:c.1179T>C	ENSP00000496760.1:p.Ile393=
ENST00000645194.1:c.1161T>C	ENSP00000496093.1:p.Ile387=
ENST00000645303.1:c.1203T>C	ENSP00000496667.1:p.Ile401=
ENST00000645634.1:c.1161T>C	ENSP00000493945.1:p.Ile387=
ENST00000645892.1:n.1293T>C
ENST00000646080.1:c.1179T>C	ENSP00000494113.1:p.Ile393=
ENST00000646099.1:c.1176T>C	ENSP00000495799.1:p.Ile392=
ENST00000646167.1:c.804T>C	ENSP00000495246.1:p.Ile268=
ENST00000646585.1:n.1343T>C
ENST00000646847.1:c.1188T>C	ENSP00000493924.1:p.Ile396=
ENST00000647076.1:c.64T>C
ENST00000647104.1:c.1161T>C	ENSP00000494025.1:p.Ile387=
ENST00000647193.1:n.314T>C
ENST00000647372.1:c.1161T>C	ENSP00000495277.1:p.Ile387=
ENST00000278379.7:c.1188T>C	ENSP00000278379.3:p.Ile396=
ENST00000395750.5:c.1161T>C	ENSP00000379099.1:p.Ile387=
ENST00000395753.5:c.1161T>C	ENSP00000379102.1:p.Ile387=
ENST00000531628.1:c.341T>C
ENST00000606205.5:c.1188T>C	ENSP00000476124.1:p.Ile396=
NM_001195728.2:c.1161T>C	NP_001182657.1:p.Ile387=
NM_001252652.1:c.1161T>C	NP_001239581.1:p.Ile387=
NM_004171.3:c.1188T>C	NP_004162.2:p.Ile396=
XM_005253067.1:c.1179T>C	XP_005253124.1:p.Ile393=
XM_011520284.1:c.1236T>C	XP_011518586.1:p.Ile412=
XM_011520285.1:c.1176T>C	XP_011518587.1:p.Ile392=
XM_011520286.1:c.1236T>C	XP_011518588.1:p.Ile412=
XM_011520287.1:c.1002T>C	XP_011518589.1:p.Ile334=
XM_011520285.2:c.1176T>C	XP_011518587.1:p.Ile392=
XM_017018136.1:c.1203T>C	XP_016873625.1:p.Ile401=
XM_017018137.1:c.1161T>C	XP_016873626.1:p.Ile387=
XM_017018138.1:c.1161T>C	XP_016873627.1:p.Ile387=
XM_017018139.1:c.954T>C	XP_016873628.1:p.Ile318=
NM_004171.4:c.1188T>C MANE Select	NP_004162.2:p.Ile396=
NM_001195728.3:c.1161T>C	NP_001182657.1:p.Ile387=
NM_001252652.2:c.1161T>C	NP_001239581.1:p.Ile387=