Canonical Allele Identifier: CA1963640078
Gene: SLC1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35286822T= , CM000673.2:g.35286822T= GRCh38
NC_000011.9:g.35308369T= , CM000673.1:g.35308369T= GRCh37
NC_000011.8:g.35264945T= NCBI36
NG_008727.1:g.137737A=
NG_008727.2:g.137737A=

Transcript Alleles

HGVS Amino-acid change
ENST00000278379.9:c.1221A= MANE Select ENSP00000278379.3:p.Val407=
ENST00000395750.6:c.1209A= ENSP00000379099.2:p.Val403=
ENST00000395753.6:c.1194A= ENSP00000379102.1:p.Val398=
ENST00000449068.2:c.1221A= ENSP00000406133.2:p.Val407=
ENST00000479543.2:n.773A=
ENST00000531628.2:c.1221A= ENSP00000436029.2:p.Val407=
ENST00000606205.6:c.1221A= ENSP00000476124.2:p.Val407=
ENST00000642171.1:c.1221A= ENSP00000495538.1:p.Val407=
ENST00000642183.1:n.1249A=
ENST00000642216.1:n.769A=
ENST00000642224.1:n.1383A=
ENST00000642448.1:n.1313A=
ENST00000642578.1:c.1194A= ENSP00000494076.1:p.Val398=
ENST00000642769.1:c.487A=
ENST00000643000.1:c.1194A= ENSP00000495164.1:p.Val398=
ENST00000643134.1:c.1221A= ENSP00000495188.1:p.Val407=
ENST00000643305.1:c.1221A= ENSP00000494828.1:p.Val407=
ENST00000643454.1:c.1212A= ENSP00000495126.1:p.Val404=
ENST00000643522.1:c.987A= ENSP00000496375.1:p.Val329=
ENST00000644050.1:c.1194A= ENSP00000496123.1:p.Val398=
ENST00000644299.1:c.1194A= ENSP00000494669.1:p.Val398=
ENST00000644351.1:c.1221A= ENSP00000496587.1:p.Val407=
ENST00000644459.1:c.1221A= ENSP00000495861.1:p.Val407=
ENST00000644779.1:c.1332A= ENSP00000494258.1:p.Val444=
ENST00000644868.1:c.1212A= ENSP00000496760.1:p.Val404=
ENST00000645194.1:c.1194A= ENSP00000496093.1:p.Val398=
ENST00000645303.1:c.1236A= ENSP00000496667.1:p.Val412=
ENST00000645634.1:c.1194A= ENSP00000493945.1:p.Val398=
ENST00000645892.1:n.1326A=
ENST00000646080.1:c.1212A= ENSP00000494113.1:p.Val404=
ENST00000646099.1:c.1209A= ENSP00000495799.1:p.Val403=
ENST00000646167.1:c.837A= ENSP00000495246.1:p.Val279=
ENST00000646585.1:n.1376A=
ENST00000647076.1:c.97A=
ENST00000647104.1:c.1194A= ENSP00000494025.1:p.Val398=
ENST00000647193.1:n.347A=
ENST00000647372.1:c.1194A= ENSP00000495277.1:p.Val398=
ENST00000278379.7:c.1221A= ENSP00000278379.3:p.Val407=
ENST00000395750.5:c.1194A= ENSP00000379099.1:p.Val398=
ENST00000395753.5:c.1194A= ENSP00000379102.1:p.Val398=
ENST00000531628.1:c.374A=
ENST00000606205.5:c.1221A= ENSP00000476124.1:p.Val407=
NM_001195728.2:c.1194A= NP_001182657.1:p.Val398=
NM_001252652.1:c.1194A= NP_001239581.1:p.Val398=
NM_004171.3:c.1221A= NP_004162.2:p.Val407=
XM_005253067.1:c.1212A= XP_005253124.1:p.Val404=
XM_011520284.1:c.1269A= XP_011518586.1:p.Val423=
XM_011520285.1:c.1209A= XP_011518587.1:p.Val403=
XM_011520286.1:c.1269A= XP_011518588.1:p.Val423=
XM_011520287.1:c.1035A= XP_011518589.1:p.Val345=
XM_011520285.2:c.1209A= XP_011518587.1:p.Val403=
XM_017018136.1:c.1236A= XP_016873625.1:p.Val412=
XM_017018137.1:c.1194A= XP_016873626.1:p.Val398=
XM_017018138.1:c.1194A= XP_016873627.1:p.Val398=
XM_017018139.1:c.987A= XP_016873628.1:p.Val329=
NM_004171.4:c.1221A= MANE Select NP_004162.2:p.Val407=
NM_001195728.3:c.1194A= NP_001182657.1:p.Val398=
NM_001252652.2:c.1194A= NP_001239581.1:p.Val398=