Canonical Allele Identifier: CA1963610910
Gene: SLC1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35260927A= , CM000673.2:g.35260927A= GRCh38
NC_000011.9:g.35282474A= , CM000673.1:g.35282474A= GRCh37
NC_000011.8:g.35239050A= NCBI36
NG_008727.1:g.163632T=
NG_008727.2:g.163632T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278379.9:c.1692T= MANE Select ENSP00000278379.3:p.Ser564=
ENST00000395750.6:c.1680T= ENSP00000379099.2:p.Ser560=
ENST00000395753.6:c.1665T= ENSP00000379102.1:p.Ser555=
ENST00000479543.2:n.1244T=
ENST00000642171.1:c.*74T= ENSP00000495538.1:n.*74T=
ENST00000642448.1:n.1784T=
ENST00000642769.1:c.958T=
ENST00000643000.1:c.1665T= ENSP00000495164.1:p.Ser555=
ENST00000643134.1:c.1679T= ENSP00000495188.1:p.Val560=
ENST00000643522.1:c.1458T= ENSP00000496375.1:p.Ser486=
ENST00000644050.1:c.1665T= ENSP00000496123.1:p.Ser555=
ENST00000644299.1:c.1665T= ENSP00000494669.1:p.Ser555=
ENST00000644459.1:c.*184T= ENSP00000495861.1:n.*184T=
ENST00000644779.1:c.1803T= ENSP00000494258.1:p.Ser601=
ENST00000644868.1:c.1754T= ENSP00000496760.1:n.1754T=
ENST00000645194.1:c.1665T= ENSP00000496093.1:p.Ser555=
ENST00000645303.1:c.1707T= ENSP00000496667.1:p.Ser569=
ENST00000645542.1:n.398T=
ENST00000645634.1:c.1665T= ENSP00000493945.1:p.Ser555=
ENST00000646080.1:c.1683T= ENSP00000494113.1:p.Ser561=
ENST00000647076.1:c.433T=
ENST00000647104.1:c.1665T= ENSP00000494025.1:p.Ser555=
ENST00000278379.7:c.1692T= ENSP00000278379.3:p.Ser564=
ENST00000395750.5:c.1665T= ENSP00000379099.1:p.Ser555=
ENST00000395753.5:c.1665T= ENSP00000379102.1:p.Ser555=
ENST00000464522.2:c.219+4600T= ENSP00000435406.1:n.219+4600T=
ENST00000479543.1:n.508T=
NM_001195728.2:c.1665T= NP_001182657.1:p.Ser555=
NM_001252652.1:c.1665T= NP_001239581.1:p.Ser555=
NM_004171.3:c.1692T= NP_004162.2:p.Ser564=
XM_005253067.1:c.1683T= XP_005253124.1:p.Ser561=
XM_011520284.1:c.1740T= XP_011518586.1:p.Ser580=
XM_011520285.1:c.1680T= XP_011518587.1:p.Ser560=
XM_011520286.1:c.1605T= XP_011518588.1:p.Ser535=
XM_011520287.1:c.1506T= XP_011518589.1:p.Ser502=
XM_011520285.2:c.1680T= XP_011518587.1:p.Ser560=
XM_017018136.1:c.1707T= XP_016873625.1:p.Ser569=
XM_017018137.1:c.1665T= XP_016873626.1:p.Ser555=
XM_017018138.1:c.1665T= XP_016873627.1:p.Ser555=
XM_017018139.1:c.1458T= XP_016873628.1:p.Ser486=
NM_004171.4:c.1692T= MANE Select NP_004162.2:p.Ser564=
NM_001195728.3:c.1665T= NP_001182657.1:p.Ser555=
NM_001252652.2:c.1665T= NP_001239581.1:p.Ser555=