Canonical Allele Identifier: CA1963611003

Gene: SLC1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35261004_35261005delinsCG , CM000673.2:g.35261004_35261005delinsCG	GRCh38
NC_000011.9:g.35282551_35282552delinsCG , CM000673.1:g.35282551_35282552delinsCG	GRCh37
NC_000011.8:g.35239127_35239128delinsCG	NCBI36
NG_008727.1:g.163554_163555delinsCG
NG_008727.2:g.163554_163555delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1654-40_1654-39delinsCG MANE Select	ENSP00000278379.3:n.1654-40_1654-39delinsCG
ENST00000395750.6:c.1642-40_1642-39delinsCG	ENSP00000379099.2:n.1642-40_1642-39delinsCG
ENST00000395753.6:c.1627-40_1627-39delinsCG	ENSP00000379102.1:n.1627-40_1627-39delinsCG
ENST00000479543.2:n.1206-40_1206-39delinsCG
ENST00000642171.1:c.*36-40_*36-39delinsCG	ENSP00000495538.1:n.*36-40_*36-39delinsCG
ENST00000642448.1:n.1746-40_1746-39delinsCG
ENST00000642769.1:c.920-40_920-39delinsCG
ENST00000643000.1:c.1627-40_1627-39delinsCG	ENSP00000495164.1:n.1627-40_1627-39delinsCG
ENST00000643134.1:c.1654-53_1654-52delinsCG	ENSP00000495188.1:n.1654-53_1654-52delinsCG
ENST00000643522.1:c.1420-40_1420-39delinsCG	ENSP00000496375.1:n.1420-40_1420-39delinsCG
ENST00000644050.1:c.1627-40_1627-39delinsCG	ENSP00000496123.1:n.1627-40_1627-39delinsCG
ENST00000644299.1:c.1627-40_1627-39delinsCG	ENSP00000494669.1:n.1627-40_1627-39delinsCG
ENST00000644459.1:c.*146-40_*146-39delinsCG	ENSP00000495861.1:n.*146-40_*146-39delinsCG
ENST00000644779.1:c.1765-40_1765-39delinsCG	ENSP00000494258.1:n.1765-40_1765-39delinsCG
ENST00000644868.1:c.1716-40_1716-39delinsCG	ENSP00000496760.1:n.1716-40_1716-39delinsCG
ENST00000645194.1:c.1627-40_1627-39delinsCG	ENSP00000496093.1:n.1627-40_1627-39delinsCG
ENST00000645303.1:c.1669-40_1669-39delinsCG	ENSP00000496667.1:n.1669-40_1669-39delinsCG
ENST00000645542.1:n.360-40_360-39delinsCG
ENST00000645634.1:c.1627-40_1627-39delinsCG	ENSP00000493945.1:n.1627-40_1627-39delinsCG
ENST00000646080.1:c.1645-40_1645-39delinsCG	ENSP00000494113.1:n.1645-40_1645-39delinsCG
ENST00000647076.1:c.395-40_395-39delinsCG
ENST00000647104.1:c.1627-40_1627-39delinsCG	ENSP00000494025.1:n.1627-40_1627-39delinsCG
ENST00000278379.7:c.1654-40_1654-39delinsCG	ENSP00000278379.3:n.1654-40_1654-39delinsCG
ENST00000395750.5:c.1627-40_1627-39delinsCG	ENSP00000379099.1:n.1627-40_1627-39delinsCG
ENST00000395753.5:c.1627-40_1627-39delinsCG	ENSP00000379102.1:n.1627-40_1627-39delinsCG
ENST00000464522.2:c.219+4522_219+4523delinsCG	ENSP00000435406.1:n.219+4522_219+4523delinsCG
ENST00000479543.1:n.470-40_470-39delinsCG
NM_001195728.2:c.1627-40_1627-39delinsCG	NP_001182657.1:n.1627-40_1627-39delinsCG
NM_001252652.1:c.1627-40_1627-39delinsCG	NP_001239581.1:n.1627-40_1627-39delinsCG
NM_004171.3:c.1654-40_1654-39delinsCG	NP_004162.2:n.1654-40_1654-39delinsCG
XM_005253067.1:c.1645-40_1645-39delinsCG	XP_005253124.1:n.1645-40_1645-39delinsCG
XM_011520284.1:c.1702-40_1702-39delinsCG	XP_011518586.1:n.1702-40_1702-39delinsCG
XM_011520285.1:c.1642-40_1642-39delinsCG	XP_011518587.1:n.1642-40_1642-39delinsCG
XM_011520286.1:c.1567-40_1567-39delinsCG	XP_011518588.1:n.1567-40_1567-39delinsCG
XM_011520287.1:c.1468-40_1468-39delinsCG	XP_011518589.1:n.1468-40_1468-39delinsCG
XM_011520285.2:c.1642-40_1642-39delinsCG	XP_011518587.1:n.1642-40_1642-39delinsCG
XM_017018136.1:c.1669-40_1669-39delinsCG	XP_016873625.1:n.1669-40_1669-39delinsCG
XM_017018137.1:c.1627-40_1627-39delinsCG	XP_016873626.1:n.1627-40_1627-39delinsCG
XM_017018138.1:c.1627-40_1627-39delinsCG	XP_016873627.1:n.1627-40_1627-39delinsCG
XM_017018139.1:c.1420-40_1420-39delinsCG	XP_016873628.1:n.1420-40_1420-39delinsCG
NM_004171.4:c.1654-40_1654-39delinsCG MANE Select	NP_004162.2:n.1654-40_1654-39delinsCG
NM_001195728.3:c.1627-40_1627-39delinsCG	NP_001182657.1:n.1627-40_1627-39delinsCG
NM_001252652.2:c.1627-40_1627-39delinsCG	NP_001239581.1:n.1627-40_1627-39delinsCG