Canonical Allele Identifier: CA1963638915

Gene: SLC1A2

Linked Data

• dbSNP Id: rs1853727849

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35362883_35362885del , CM000673.2:g.35362883_35362885del	GRCh38
NC_000011.9:g.35384430_35384432del , CM000673.1:g.35384430_35384432del	GRCh37
NC_000011.8:g.35341006_35341008del	NCBI36
NG_008727.1:g.61674_61676del
NG_008727.2:g.61674_61676del

Transcript Alleles

HGVS	Amino-acid change
ENST00000278379.9:c.18-45369_18-45367del MANE Select	ENSP00000278379.3:n.18-45369_18-45367del
ENST00000395750.6:c.6-45369_6-45367del	ENSP00000379099.2:n.6-45369_6-45367del
ENST00000395753.6:c.-10-45369_-10-45367del	ENSP00000379102.1:n.-10-45369_-10-45367del
ENST00000449068.2:c.18-45369_18-45367del	ENSP00000406133.2:n.18-45369_18-45367del
ENST00000531628.2:c.18-45369_18-45367del	ENSP00000436029.2:n.18-45369_18-45367del
ENST00000606205.6:c.18-45369_18-45367del	ENSP00000476124.2:n.18-45369_18-45367del
ENST00000642171.1:c.18-45369_18-45367del	ENSP00000495538.1:n.18-45369_18-45367del
ENST00000642183.1:n.279+36690_279+36692del
ENST00000642224.1:n.306+36690_306+36692del
ENST00000642392.1:n.90-45369_90-45367del
ENST00000642448.1:n.110-45369_110-45367del
ENST00000642578.1:c.-10-45369_-10-45367del	ENSP00000494076.1:n.-10-45369_-10-45367del
ENST00000643000.1:c.-10-45369_-10-45367del	ENSP00000495164.1:n.-10-45369_-10-45367del
ENST00000643134.1:c.18-45369_18-45367del	ENSP00000495188.1:n.18-45369_18-45367del
ENST00000643154.1:n.598-45369_598-45367del
ENST00000643305.1:c.18-45369_18-45367del	ENSP00000494828.1:n.18-45369_18-45367del
ENST00000643401.1:c.34-40206_34-40204del	ENSP00000493765.1:n.34-40206_34-40204del
ENST00000643522.1:c.18-45369_18-45367del	ENSP00000496375.1:n.18-45369_18-45367del
ENST00000644050.1:c.-129-40206_-129-40204del	ENSP00000496123.1:n.-129-40206_-129-40204del
ENST00000644299.1:c.-10-45369_-10-45367del	ENSP00000494669.1:n.-10-45369_-10-45367del
ENST00000644351.1:c.18-45369_18-45367del	ENSP00000496587.1:n.18-45369_18-45367del
ENST00000644459.1:c.18-45369_18-45367del	ENSP00000495861.1:n.18-45369_18-45367del
ENST00000644779.1:c.-536-39576_-536-39574del	ENSP00000494258.1:n.-536-39576_-536-39574del
ENST00000645194.1:c.-10-45369_-10-45367del	ENSP00000496093.1:n.-10-45369_-10-45367del
ENST00000645303.1:c.32+17496_32+17498del	ENSP00000496667.1:n.32+17496_32+17498del
ENST00000645634.1:c.-11+8056_-11+8058del	ENSP00000493945.1:n.-11+8056_-11+8058del
ENST00000645966.1:c.-11+28655_-11+28657del	ENSP00000493762.1:n.-11+28655_-11+28657del
ENST00000646099.1:c.6-45369_6-45367del	ENSP00000495799.1:n.6-45369_6-45367del
ENST00000646585.1:n.172+41434_172+41436del
ENST00000646847.1:c.18-45369_18-45367del	ENSP00000493924.1:n.18-45369_18-45367del
ENST00000647104.1:c.-129-40206_-129-40204del	ENSP00000494025.1:n.-129-40206_-129-40204del
ENST00000647372.1:c.-10-45369_-10-45367del	ENSP00000495277.1:n.-10-45369_-10-45367del
ENST00000278379.7:c.18-45369_18-45367del	ENSP00000278379.3:n.18-45369_18-45367del
ENST00000395750.5:c.-129-40206_-129-40204del	ENSP00000379099.1:n.-129-40206_-129-40204del
ENST00000395753.5:c.-11+8056_-11+8058del	ENSP00000379102.1:n.-11+8056_-11+8058del
ENST00000449068.1:c.6-45369_6-45367del	ENSP00000406133.1:n.6-45369_6-45367del
ENST00000606205.5:c.18-45369_18-45367del	ENSP00000476124.1:n.18-45369_18-45367del
NM_001195728.2:c.-129-40206_-129-40204del	NP_001182657.1:n.-129-40206_-129-40204del
NM_001252652.1:c.-11+8056_-11+8058del	NP_001239581.1:n.-11+8056_-11+8058del
NM_004171.3:c.18-45369_18-45367del	NP_004162.2:n.18-45369_18-45367del
XM_011520284.1:c.65+36690_65+36692del	XP_011518586.1:n.65+36690_65+36692del
XM_011520285.1:c.6-45369_6-45367del	XP_011518587.1:n.6-45369_6-45367del
XM_011520286.1:c.65+36690_65+36692del	XP_011518588.1:n.65+36690_65+36692del
XM_011520287.1:c.65+36690_65+36692del	XP_011518589.1:n.65+36690_65+36692del
XM_011520285.2:c.6-45369_6-45367del	XP_011518587.1:n.6-45369_6-45367del
XM_017018136.1:c.32+17496_32+17498del	XP_016873625.1:n.32+17496_32+17498del
XM_017018137.1:c.-10-45369_-10-45367del	XP_016873626.1:n.-10-45369_-10-45367del
XM_017018138.1:c.-10-45369_-10-45367del	XP_016873627.1:n.-10-45369_-10-45367del
XM_017018139.1:c.18-45369_18-45367del	XP_016873628.1:n.18-45369_18-45367del
NM_004171.4:c.18-45369_18-45367del MANE Select	NP_004162.2:n.18-45369_18-45367del
NM_001195728.3:c.-129-40206_-129-40204del	NP_001182657.1:n.-129-40206_-129-40204del
NM_001252652.2:c.-11+8056_-11+8058del	NP_001239581.1:n.-11+8056_-11+8058del