Canonical Allele Identifier: CA598532069

Gene: SLC1A2

Linked Data

• dbSNP Id: rs1236603189
• gnomAD v2: 11-35282434-C-T
• gnomAD v4: 11-35260887-C-T
• MyVariant Identifiers: chr11:g.35282434C>T (hg19) ; chr11:g.35260887C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260887C>T , CM000673.2:g.35260887C>T	GRCh38
NC_000011.9:g.35282434C>T , CM000673.1:g.35282434C>T	GRCh37
NC_000011.8:g.35239010C>T	NCBI36
NG_008727.1:g.163672G>A
NG_008727.2:g.163672G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.*7G>A MANE Select	ENSP00000278379.3:n.*7G>A
ENST00000395750.6:c.*7G>A	ENSP00000379099.2:n.*7G>A
ENST00000395753.6:c.*7G>A	ENSP00000379102.1:n.*7G>A
ENST00000479543.2:n.1284G>A
ENST00000642171.1:c.*114G>A	ENSP00000495538.1:n.*114G>A
ENST00000642448.1:n.1824G>A
ENST00000642769.1:c.998G>A
ENST00000643000.1:c.*7G>A	ENSP00000495164.1:n.*7G>A
ENST00000643134.1:c.1719G>A	ENSP00000495188.1:p.Met573Ile
ENST00000643522.1:c.*7G>A	ENSP00000496375.1:n.*7G>A
ENST00000644050.1:c.*7G>A	ENSP00000496123.1:n.*7G>A
ENST00000644299.1:c.*7G>A	ENSP00000494669.1:n.*7G>A
ENST00000644459.1:c.*224G>A	ENSP00000495861.1:n.*224G>A
ENST00000644779.1:c.*7G>A	ENSP00000494258.1:n.*7G>A
ENST00000644868.1:c.1794G>A	ENSP00000496760.1:n.1794G>A
ENST00000645194.1:c.*7G>A	ENSP00000496093.1:n.*7G>A
ENST00000645303.1:c.*7G>A	ENSP00000496667.1:n.*7G>A
ENST00000645542.1:n.438G>A
ENST00000645634.1:c.*7G>A	ENSP00000493945.1:n.*7G>A
ENST00000646080.1:c.*7G>A	ENSP00000494113.1:n.*7G>A
ENST00000647076.1:c.473G>A
ENST00000647104.1:c.*7G>A	ENSP00000494025.1:n.*7G>A
ENST00000278379.7:c.*7G>A	ENSP00000278379.3:n.*7G>A
ENST00000395750.5:c.*7G>A	ENSP00000379099.1:n.*7G>A
ENST00000395753.5:c.*7G>A	ENSP00000379102.1:n.*7G>A
ENST00000464522.2:c.219+4640G>A	ENSP00000435406.1:n.219+4640G>A
ENST00000479543.1:n.548G>A
NM_001195728.2:c.*7G>A	NP_001182657.1:n.*7G>A
NM_001252652.1:c.*7G>A	NP_001239581.1:n.*7G>A
NM_004171.3:c.*7G>A	NP_004162.2:n.*7G>A
XM_005253067.1:c.*7G>A	XP_005253124.1:n.*7G>A
XM_011520284.1:c.*7G>A	XP_011518586.1:n.*7G>A
XM_011520285.1:c.*7G>A	XP_011518587.1:n.*7G>A
XM_011520286.1:c.*7G>A	XP_011518588.1:n.*7G>A
XM_011520287.1:c.*7G>A	XP_011518589.1:n.*7G>A
XM_011520285.2:c.*7G>A	XP_011518587.1:n.*7G>A
XM_017018136.1:c.*7G>A	XP_016873625.1:n.*7G>A
XM_017018137.1:c.*7G>A	XP_016873626.1:n.*7G>A
XM_017018138.1:c.*7G>A	XP_016873627.1:n.*7G>A
XM_017018139.1:c.*7G>A	XP_016873628.1:n.*7G>A
NM_004171.4:c.*7G>A MANE Select	NP_004162.2:n.*7G>A
NM_001195728.3:c.*7G>A	NP_001182657.1:n.*7G>A
NM_001252652.2:c.*7G>A	NP_001239581.1:n.*7G>A