Canonical Allele Identifier: CA1963676148

Gene: SLC1A2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35392417C>A , CM000673.2:g.35392417C>A	GRCh38
NC_000011.9:g.35413964C>A , CM000673.1:g.35413964C>A	GRCh37
NC_000011.8:g.35370540C>A	NCBI36
NG_008727.1:g.32142G>T
NG_008727.2:g.32142G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.17+26533G>T MANE Select	ENSP00000278379.3:n.17+26533G>T
ENST00000395750.6:c.5+27519G>T	ENSP00000379099.2:n.5+27519G>T
ENST00000395753.6:c.-11+27491G>T	ENSP00000379102.1:n.-11+27491G>T
ENST00000449068.2:c.17+26533G>T	ENSP00000406133.2:n.17+26533G>T
ENST00000531628.2:c.17+26533G>T	ENSP00000436029.2:n.17+26533G>T
ENST00000606205.6:c.17+26533G>T	ENSP00000476124.2:n.17+26533G>T
ENST00000642171.1:c.17+26533G>T	ENSP00000495538.1:n.17+26533G>T
ENST00000642183.1:n.279+7158G>T
ENST00000642224.1:n.306+7158G>T
ENST00000642392.1:n.89+27519G>T
ENST00000642448.1:n.109+21271G>T
ENST00000642578.1:c.-11+27491G>T	ENSP00000494076.1:n.-11+27491G>T
ENST00000643000.1:c.-11+27503G>T	ENSP00000495164.1:n.-11+27503G>T
ENST00000643134.1:c.17+26533G>T	ENSP00000495188.1:n.17+26533G>T
ENST00000643154.1:n.597+26533G>T
ENST00000643305.1:c.17+26533G>T	ENSP00000494828.1:n.17+26533G>T
ENST00000643401.1:c.33+27491G>T	ENSP00000493765.1:n.33+27491G>T
ENST00000643522.1:c.17+26533G>T	ENSP00000496375.1:n.17+26533G>T
ENST00000644050.1:c.-130+26533G>T	ENSP00000496123.1:n.-130+26533G>T
ENST00000644100.1:n.93-11886G>T
ENST00000644299.1:c.-11+26063G>T	ENSP00000494669.1:n.-11+26063G>T
ENST00000644351.1:c.17+26533G>T	ENSP00000496587.1:n.17+26533G>T
ENST00000644459.1:c.17+26533G>T	ENSP00000495861.1:n.17+26533G>T
ENST00000644779.1:c.-537+26533G>T	ENSP00000494258.1:n.-537+26533G>T
ENST00000645194.1:c.-11+25932G>T	ENSP00000496093.1:n.-11+25932G>T
ENST00000645303.1:c.-129-11876G>T	ENSP00000496667.1:n.-129-11876G>T
ENST00000645634.1:c.-166-21321G>T	ENSP00000493945.1:n.-166-21321G>T
ENST00000645966.1:c.-79-809G>T	ENSP00000493762.1:n.-79-809G>T
ENST00000646099.1:c.5+27519G>T	ENSP00000495799.1:n.5+27519G>T
ENST00000646585.1:n.172+11902G>T
ENST00000646847.1:c.17+26533G>T	ENSP00000493924.1:n.17+26533G>T
ENST00000647104.1:c.-130+27519G>T	ENSP00000494025.1:n.-130+27519G>T
ENST00000647372.1:c.-11+27503G>T	ENSP00000495277.1:n.-11+27503G>T
ENST00000278379.7:c.17+26533G>T	ENSP00000278379.3:n.17+26533G>T
ENST00000395750.5:c.-130+27519G>T	ENSP00000379099.1:n.-130+27519G>T
ENST00000395753.5:c.-166-21321G>T	ENSP00000379102.1:n.-166-21321G>T
ENST00000449068.1:c.5+27519G>T	ENSP00000406133.1:n.5+27519G>T
ENST00000606205.5:c.17+26533G>T	ENSP00000476124.1:n.17+26533G>T
NM_001195728.2:c.-130+27519G>T	NP_001182657.1:n.-130+27519G>T
NM_001252652.1:c.-166-21321G>T	NP_001239581.1:n.-166-21321G>T
NM_004171.3:c.17+26533G>T	NP_004162.2:n.17+26533G>T
XM_011520284.1:c.65+7158G>T	XP_011518586.1:n.65+7158G>T
XM_011520285.1:c.5+27519G>T	XP_011518587.1:n.5+27519G>T
XM_011520286.1:c.65+7158G>T	XP_011518588.1:n.65+7158G>T
XM_011520287.1:c.65+7158G>T	XP_011518589.1:n.65+7158G>T
XM_011520285.2:c.5+27519G>T	XP_011518587.1:n.5+27519G>T
XM_017018137.1:c.-11+27491G>T	XP_016873626.1:n.-11+27491G>T
XM_017018138.1:c.-11+27503G>T	XP_016873627.1:n.-11+27503G>T
XM_017018139.1:c.17+26533G>T	XP_016873628.1:n.17+26533G>T
NM_004171.4:c.17+26533G>T MANE Select	NP_004162.2:n.17+26533G>T
NM_001195728.3:c.-130+27519G>T	NP_001182657.1:n.-130+27519G>T
NM_001252652.2:c.-166-21321G>T	NP_001239581.1:n.-166-21321G>T