Canonical Allele Identifier: CA473548902

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282448del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260901del , CM000673.2:g.35260901del	GRCh38
NC_000011.9:g.35282448del , CM000673.1:g.35282448del	GRCh37
NC_000011.8:g.35239024del	NCBI36
NG_008727.1:g.163658del
NG_008727.2:g.163658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1718del MANE Select	ENSP00000278379.3:p.Glu573GlyfsTer22
ENST00000395750.6:c.1706del	ENSP00000379099.2:p.Glu569GlyfsTer22
ENST00000395753.6:c.1691del	ENSP00000379102.1:p.Glu564GlyfsTer22
ENST00000479543.2:n.1270del
ENST00000642171.1:c.*100del	ENSP00000495538.1:n.*100del
ENST00000642448.1:n.1810del
ENST00000642769.1:c.984del
ENST00000643000.1:c.1691del	ENSP00000495164.1:p.Glu564GlyfsTer22
ENST00000643134.1:c.1705del	ENSP00000495188.1:p.Arg569GlufsTer5
ENST00000643522.1:c.1484del	ENSP00000496375.1:p.Glu495GlyfsTer22
ENST00000644050.1:c.1691del	ENSP00000496123.1:p.Glu564GlyfsTer22
ENST00000644299.1:c.1691del	ENSP00000494669.1:p.Glu564GlyfsTer22
ENST00000644459.1:c.*210del	ENSP00000495861.1:n.*210del
ENST00000644779.1:c.1829del	ENSP00000494258.1:p.Glu610GlyfsTer22
ENST00000644868.1:c.1780del	ENSP00000496760.1:n.1780del
ENST00000645194.1:c.1691del	ENSP00000496093.1:p.Glu564GlyfsTer22
ENST00000645303.1:c.1733del	ENSP00000496667.1:p.Glu578GlyfsTer22
ENST00000645542.1:n.424del
ENST00000645634.1:c.1691del	ENSP00000493945.1:p.Glu564GlyfsTer22
ENST00000646080.1:c.1709del	ENSP00000494113.1:p.Glu570GlyfsTer22
ENST00000647076.1:c.459del
ENST00000647104.1:c.1691del	ENSP00000494025.1:p.Glu564GlyfsTer22
ENST00000278379.7:c.1718del	ENSP00000278379.3:p.Glu573GlyfsTer22
ENST00000395750.5:c.1691del	ENSP00000379099.1:p.Glu564GlyfsTer22
ENST00000395753.5:c.1691del	ENSP00000379102.1:p.Glu564GlyfsTer22
ENST00000464522.2:c.219+4626del	ENSP00000435406.1:n.219+4626del
ENST00000479543.1:n.534del
NM_001195728.2:c.1691del	NP_001182657.1:p.Glu564GlyfsTer22
NM_001252652.1:c.1691del	NP_001239581.1:p.Glu564GlyfsTer22
NM_004171.3:c.1718del	NP_004162.2:p.Glu573GlyfsTer22
XM_005253067.1:c.1709del	XP_005253124.1:p.Glu570GlyfsTer22
XM_011520284.1:c.1766del	XP_011518586.1:p.Glu589GlyfsTer22
XM_011520285.1:c.1706del	XP_011518587.1:p.Glu569GlyfsTer22
XM_011520286.1:c.1631del	XP_011518588.1:p.Glu544GlyfsTer22
XM_011520287.1:c.1532del	XP_011518589.1:p.Glu511GlyfsTer22
XM_011520285.2:c.1706del	XP_011518587.1:p.Glu569GlyfsTer22
XM_017018136.1:c.1733del	XP_016873625.1:p.Glu578GlyfsTer22
XM_017018137.1:c.1691del	XP_016873626.1:p.Glu564GlyfsTer22
XM_017018138.1:c.1691del	XP_016873627.1:p.Glu564GlyfsTer22
XM_017018139.1:c.1484del	XP_016873628.1:p.Glu495GlyfsTer22
NM_004171.4:c.1718del MANE Select	NP_004162.2:p.Glu573GlyfsTer22
NM_001195728.3:c.1691del	NP_001182657.1:p.Glu564GlyfsTer22
NM_001252652.2:c.1691del	NP_001239581.1:p.Glu564GlyfsTer22