Canonical Allele Identifier: CA675896101

Gene: SLC1A2

Linked Data

• dbSNP Id: rs1410497856
• MyVariant Identifiers: chr11:g.35329565del (hg19) ; chr11:g.35308018del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35308018del , CM000673.2:g.35308018del	GRCh38
NC_000011.9:g.35329565del , CM000673.1:g.35329565del	GRCh37
NC_000011.8:g.35286141del	NCBI36
NG_008727.1:g.116541del
NG_008727.2:g.116541del

Transcript Alleles

HGVS	Amino-acid change
ENST00000278379.9:c.562-1776del MANE Select	ENSP00000278379.3:n.562-1776del
ENST00000395750.6:c.550-1776del	ENSP00000379099.2:n.550-1776del
ENST00000395753.6:c.535-1776del	ENSP00000379102.1:n.535-1776del
ENST00000449068.2:c.562-1776del	ENSP00000406133.2:n.562-1776del
ENST00000531628.2:c.562-1776del	ENSP00000436029.2:n.562-1776del
ENST00000606205.6:c.562-1776del	ENSP00000476124.2:n.562-1776del
ENST00000642171.1:c.562-1776del	ENSP00000495538.1:n.562-1776del
ENST00000642183.1:n.824-1776del
ENST00000642224.1:n.851-1776del
ENST00000642448.1:n.654-1776del
ENST00000642578.1:c.535-1776del	ENSP00000494076.1:n.535-1776del
ENST00000643000.1:c.535-1776del	ENSP00000495164.1:n.535-1776del
ENST00000643134.1:c.562-1776del	ENSP00000495188.1:n.562-1776del
ENST00000643154.1:n.1142-1776del
ENST00000643305.1:c.562-1776del	ENSP00000494828.1:n.562-1776del
ENST00000643454.1:c.553-1776del	ENSP00000495126.1:n.553-1776del
ENST00000643522.1:c.562-1776del	ENSP00000496375.1:n.562-1776del
ENST00000644050.1:c.535-1776del	ENSP00000496123.1:n.535-1776del
ENST00000644299.1:c.535-1776del	ENSP00000494669.1:n.535-1776del
ENST00000644351.1:c.562-1776del	ENSP00000496587.1:n.562-1776del
ENST00000644459.1:c.562-1776del	ENSP00000495861.1:n.562-1776del
ENST00000644779.1:c.673-1776del	ENSP00000494258.1:n.673-1776del
ENST00000644868.1:c.553-1776del	ENSP00000496760.1:n.553-1776del
ENST00000645194.1:c.535-1776del	ENSP00000496093.1:n.535-1776del
ENST00000645303.1:c.577-1776del	ENSP00000496667.1:n.577-1776del
ENST00000645634.1:c.535-1776del	ENSP00000493945.1:n.535-1776del
ENST00000645892.1:n.667-1776del
ENST00000646080.1:c.553-1776del	ENSP00000494113.1:n.553-1776del
ENST00000646099.1:c.550-1776del	ENSP00000495799.1:n.550-1776del
ENST00000646112.1:n.644-1776del
ENST00000646167.1:c.412-1776del	ENSP00000495246.1:n.412-1776del
ENST00000646585.1:n.717-1776del
ENST00000646847.1:c.562-1776del	ENSP00000493924.1:n.562-1776del
ENST00000647104.1:c.535-1776del	ENSP00000494025.1:n.535-1776del
ENST00000647372.1:c.535-1776del	ENSP00000495277.1:n.535-1776del
ENST00000278379.7:c.562-1776del	ENSP00000278379.3:n.562-1776del
ENST00000395750.5:c.535-1776del	ENSP00000379099.1:n.535-1776del
ENST00000395753.5:c.535-1776del	ENSP00000379102.1:n.535-1776del
ENST00000449068.1:c.550-1776del	ENSP00000406133.1:n.550-1776del
ENST00000606205.5:c.562-1776del	ENSP00000476124.1:n.562-1776del
NM_001195728.2:c.535-1776del	NP_001182657.1:n.535-1776del
NM_001252652.1:c.535-1776del	NP_001239581.1:n.535-1776del
NM_004171.3:c.562-1776del	NP_004162.2:n.562-1776del
XM_005253067.1:c.553-1776del	XP_005253124.1:n.553-1776del
XM_011520284.1:c.610-1776del	XP_011518586.1:n.610-1776del
XM_011520285.1:c.550-1776del	XP_011518587.1:n.550-1776del
XM_011520286.1:c.610-1776del	XP_011518588.1:n.610-1776del
XM_011520287.1:c.610-1776del	XP_011518589.1:n.610-1776del
XM_011520285.2:c.550-1776del	XP_011518587.1:n.550-1776del
XM_017018136.1:c.577-1776del	XP_016873625.1:n.577-1776del
XM_017018137.1:c.535-1776del	XP_016873626.1:n.535-1776del
XM_017018138.1:c.535-1776del	XP_016873627.1:n.535-1776del
XM_017018139.1:c.562-1776del	XP_016873628.1:n.562-1776del
NM_004171.4:c.562-1776del MANE Select	NP_004162.2:n.562-1776del
NM_001195728.3:c.535-1776del	NP_001182657.1:n.535-1776del
NM_001252652.2:c.535-1776del	NP_001239581.1:n.535-1776del