Canonical Allele Identifier: CA380124642

Gene: SLC1A2

Linked Data

• gnomAD v4: 11-35260914-G-T
• MyVariant Identifiers: chr11:g.35282461G>T (hg19) ; chr11:g.35260914G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260914G>T , CM000673.2:g.35260914G>T	GRCh38
NC_000011.9:g.35282461G>T , CM000673.1:g.35282461G>T	GRCh37
NC_000011.8:g.35239037G>T	NCBI36
NG_008727.1:g.163645C>A
NG_008727.2:g.163645C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1705C>A MANE Select	ENSP00000278379.3:p.Pro569Thr
ENST00000395750.6:c.1693C>A	ENSP00000379099.2:p.Pro565Thr
ENST00000395753.6:c.1678C>A	ENSP00000379102.1:p.Pro560Thr
ENST00000479543.2:n.1257C>A
ENST00000642171.1:c.*87C>A	ENSP00000495538.1:n.*87C>A
ENST00000642448.1:n.1797C>A
ENST00000642769.1:c.971C>A
ENST00000643000.1:c.1678C>A	ENSP00000495164.1:p.Pro560Thr
ENST00000643134.1:c.1692C>A	ENSP00000495188.1:p.Asn564Lys
ENST00000643522.1:c.1471C>A	ENSP00000496375.1:p.Pro491Thr
ENST00000644050.1:c.1678C>A	ENSP00000496123.1:p.Pro560Thr
ENST00000644299.1:c.1678C>A	ENSP00000494669.1:p.Pro560Thr
ENST00000644459.1:c.*197C>A	ENSP00000495861.1:n.*197C>A
ENST00000644779.1:c.1816C>A	ENSP00000494258.1:p.Pro606Thr
ENST00000644868.1:c.1767C>A	ENSP00000496760.1:n.1767C>A
ENST00000645194.1:c.1678C>A	ENSP00000496093.1:p.Pro560Thr
ENST00000645303.1:c.1720C>A	ENSP00000496667.1:p.Pro574Thr
ENST00000645542.1:n.411C>A
ENST00000645634.1:c.1678C>A	ENSP00000493945.1:p.Pro560Thr
ENST00000646080.1:c.1696C>A	ENSP00000494113.1:p.Pro566Thr
ENST00000647076.1:c.446C>A
ENST00000647104.1:c.1678C>A	ENSP00000494025.1:p.Pro560Thr
ENST00000278379.7:c.1705C>A	ENSP00000278379.3:p.Pro569Thr
ENST00000395750.5:c.1678C>A	ENSP00000379099.1:p.Pro560Thr
ENST00000395753.5:c.1678C>A	ENSP00000379102.1:p.Pro560Thr
ENST00000464522.2:c.219+4613C>A	ENSP00000435406.1:n.219+4613C>A
ENST00000479543.1:n.521C>A
NM_001195728.2:c.1678C>A	NP_001182657.1:p.Pro560Thr
NM_001252652.1:c.1678C>A	NP_001239581.1:p.Pro560Thr
NM_004171.3:c.1705C>A	NP_004162.2:p.Pro569Thr
XM_005253067.1:c.1696C>A	XP_005253124.1:p.Pro566Thr
XM_011520284.1:c.1753C>A	XP_011518586.1:p.Pro585Thr
XM_011520285.1:c.1693C>A	XP_011518587.1:p.Pro565Thr
XM_011520286.1:c.1618C>A	XP_011518588.1:p.Pro540Thr
XM_011520287.1:c.1519C>A	XP_011518589.1:p.Pro507Thr
XM_011520285.2:c.1693C>A	XP_011518587.1:p.Pro565Thr
XM_017018136.1:c.1720C>A	XP_016873625.1:p.Pro574Thr
XM_017018137.1:c.1678C>A	XP_016873626.1:p.Pro560Thr
XM_017018138.1:c.1678C>A	XP_016873627.1:p.Pro560Thr
XM_017018139.1:c.1471C>A	XP_016873628.1:p.Pro491Thr
NM_004171.4:c.1705C>A MANE Select	NP_004162.2:p.Pro569Thr
NM_001195728.3:c.1678C>A	NP_001182657.1:p.Pro560Thr
NM_001252652.2:c.1678C>A	NP_001239581.1:p.Pro560Thr