Canonical Allele Identifier: CA380124791

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282497T>C (hg19) ; chr11:g.35260950T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260950T>C , CM000673.2:g.35260950T>C	GRCh38
NC_000011.9:g.35282497T>C , CM000673.1:g.35282497T>C	GRCh37
NC_000011.8:g.35239073T>C	NCBI36
NG_008727.1:g.163609A>G
NG_008727.2:g.163609A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1669A>G MANE Select	ENSP00000278379.3:p.Asn557Asp
ENST00000395750.6:c.1657A>G	ENSP00000379099.2:p.Asn553Asp
ENST00000395753.6:c.1642A>G	ENSP00000379102.1:p.Asn548Asp
ENST00000479543.2:n.1221A>G
ENST00000642171.1:c.*51A>G	ENSP00000495538.1:n.*51A>G
ENST00000642448.1:n.1761A>G
ENST00000642769.1:c.935A>G
ENST00000643000.1:c.1642A>G	ENSP00000495164.1:p.Asn548Asp
ENST00000643134.1:c.1656A>G	ENSP00000495188.1:p.Pro552=
ENST00000643522.1:c.1435A>G	ENSP00000496375.1:p.Asn479Asp
ENST00000644050.1:c.1642A>G	ENSP00000496123.1:p.Asn548Asp
ENST00000644299.1:c.1642A>G	ENSP00000494669.1:p.Asn548Asp
ENST00000644459.1:c.*161A>G	ENSP00000495861.1:n.*161A>G
ENST00000644779.1:c.1780A>G	ENSP00000494258.1:p.Asn594Asp
ENST00000644868.1:c.1731A>G	ENSP00000496760.1:n.1731A>G
ENST00000645194.1:c.1642A>G	ENSP00000496093.1:p.Asn548Asp
ENST00000645303.1:c.1684A>G	ENSP00000496667.1:p.Asn562Asp
ENST00000645542.1:n.375A>G
ENST00000645634.1:c.1642A>G	ENSP00000493945.1:p.Asn548Asp
ENST00000646080.1:c.1660A>G	ENSP00000494113.1:p.Asn554Asp
ENST00000647076.1:c.410A>G
ENST00000647104.1:c.1642A>G	ENSP00000494025.1:p.Asn548Asp
ENST00000278379.7:c.1669A>G	ENSP00000278379.3:p.Asn557Asp
ENST00000395750.5:c.1642A>G	ENSP00000379099.1:p.Asn548Asp
ENST00000395753.5:c.1642A>G	ENSP00000379102.1:p.Asn548Asp
ENST00000464522.2:c.219+4577A>G	ENSP00000435406.1:n.219+4577A>G
ENST00000479543.1:n.485A>G
NM_001195728.2:c.1642A>G	NP_001182657.1:p.Asn548Asp
NM_001252652.1:c.1642A>G	NP_001239581.1:p.Asn548Asp
NM_004171.3:c.1669A>G	NP_004162.2:p.Asn557Asp
XM_005253067.1:c.1660A>G	XP_005253124.1:p.Asn554Asp
XM_011520284.1:c.1717A>G	XP_011518586.1:p.Asn573Asp
XM_011520285.1:c.1657A>G	XP_011518587.1:p.Asn553Asp
XM_011520286.1:c.1582A>G	XP_011518588.1:p.Asn528Asp
XM_011520287.1:c.1483A>G	XP_011518589.1:p.Asn495Asp
XM_011520285.2:c.1657A>G	XP_011518587.1:p.Asn553Asp
XM_017018136.1:c.1684A>G	XP_016873625.1:p.Asn562Asp
XM_017018137.1:c.1642A>G	XP_016873626.1:p.Asn548Asp
XM_017018138.1:c.1642A>G	XP_016873627.1:p.Asn548Asp
XM_017018139.1:c.1435A>G	XP_016873628.1:p.Asn479Asp
NM_004171.4:c.1669A>G MANE Select	NP_004162.2:p.Asn557Asp
NM_001195728.3:c.1642A>G	NP_001182657.1:p.Asn548Asp
NM_001252652.2:c.1642A>G	NP_001239581.1:p.Asn548Asp