Canonical Allele Identifier: CA2613103953

Gene: SLC1A2

Linked Data

• gnomAD v4: 11-35260888-A-ATAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260889_35260891dup , CM000673.2:g.35260889_35260891dup	GRCh38
NC_000011.9:g.35282436_35282438dup , CM000673.1:g.35282436_35282438dup	GRCh37
NC_000011.8:g.35239012_35239014dup	NCBI36
NG_008727.1:g.163668_163670dup
NG_008727.2:g.163668_163670dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.*3_*5dup MANE Select	ENSP00000278379.3:n.*3_*5dup
ENST00000395750.6:c.*3_*5dup	ENSP00000379099.2:n.*3_*5dup
ENST00000395753.6:c.*3_*5dup	ENSP00000379102.1:n.*3_*5dup
ENST00000479543.2:n.1280_1282dup
ENST00000642171.1:c.*110_*112dup	ENSP00000495538.1:n.*110_*112dup
ENST00000642448.1:n.1820_1822dup
ENST00000642769.1:c.994_996dup
ENST00000643000.1:c.*3_*5dup	ENSP00000495164.1:n.*3_*5dup
ENST00000643134.1:c.1715_1717dup	ENSP00000495188.1:p.Asp572_Met573insAsn
ENST00000643522.1:c.*3_*5dup	ENSP00000496375.1:n.*3_*5dup
ENST00000644050.1:c.*3_*5dup	ENSP00000496123.1:n.*3_*5dup
ENST00000644299.1:c.*3_*5dup	ENSP00000494669.1:n.*3_*5dup
ENST00000644459.1:c.*220_*222dup	ENSP00000495861.1:n.*220_*222dup
ENST00000644779.1:c.*3_*5dup	ENSP00000494258.1:n.*3_*5dup
ENST00000644868.1:c.1790_1792dup	ENSP00000496760.1:n.1790_1792dup
ENST00000645194.1:c.*3_*5dup	ENSP00000496093.1:n.*3_*5dup
ENST00000645303.1:c.*3_*5dup	ENSP00000496667.1:n.*3_*5dup
ENST00000645542.1:n.434_436dup
ENST00000645634.1:c.*3_*5dup	ENSP00000493945.1:n.*3_*5dup
ENST00000646080.1:c.*3_*5dup	ENSP00000494113.1:n.*3_*5dup
ENST00000647076.1:c.469_471dup
ENST00000647104.1:c.*3_*5dup	ENSP00000494025.1:n.*3_*5dup
ENST00000278379.7:c.*3_*5dup	ENSP00000278379.3:n.*3_*5dup
ENST00000395750.5:c.*3_*5dup	ENSP00000379099.1:n.*3_*5dup
ENST00000395753.5:c.*3_*5dup	ENSP00000379102.1:n.*3_*5dup
ENST00000464522.2:c.219+4636_219+4638dup	ENSP00000435406.1:n.219+4636_219+4638dup
ENST00000479543.1:n.544_546dup
NM_001195728.2:c.*3_*5dup	NP_001182657.1:n.*3_*5dup
NM_001252652.1:c.*3_*5dup	NP_001239581.1:n.*3_*5dup
NM_004171.3:c.*3_*5dup	NP_004162.2:n.*3_*5dup
XM_005253067.1:c.*3_*5dup	XP_005253124.1:n.*3_*5dup
XM_011520284.1:c.*3_*5dup	XP_011518586.1:n.*3_*5dup
XM_011520285.1:c.*3_*5dup	XP_011518587.1:n.*3_*5dup
XM_011520286.1:c.*3_*5dup	XP_011518588.1:n.*3_*5dup
XM_011520287.1:c.*3_*5dup	XP_011518589.1:n.*3_*5dup
XM_011520285.2:c.*3_*5dup	XP_011518587.1:n.*3_*5dup
XM_017018136.1:c.*3_*5dup	XP_016873625.1:n.*3_*5dup
XM_017018137.1:c.*3_*5dup	XP_016873626.1:n.*3_*5dup
XM_017018138.1:c.*3_*5dup	XP_016873627.1:n.*3_*5dup
XM_017018139.1:c.*3_*5dup	XP_016873628.1:n.*3_*5dup
NM_004171.4:c.*3_*5dup MANE Select	NP_004162.2:n.*3_*5dup
NM_001195728.3:c.*3_*5dup	NP_001182657.1:n.*3_*5dup
NM_001252652.2:c.*3_*5dup	NP_001239581.1:n.*3_*5dup