Canonical Allele Identifier: CA2613103914

Gene: SLC1A2

Linked Data

• gnomAD v4: 11-35260814-TAAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260819_35260822del , CM000673.2:g.35260819_35260822del	GRCh38
NC_000011.9:g.35282366_35282369del , CM000673.1:g.35282366_35282369del	GRCh37
NC_000011.8:g.35238942_35238945del	NCBI36
NG_008727.1:g.163741_163744del
NG_008727.2:g.163741_163744del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.*76_*79del MANE Select	ENSP00000278379.3:n.*76_*79del
ENST00000395750.6:c.*76_*79del	ENSP00000379099.2:n.*76_*79del
ENST00000395753.6:c.*76_*79del	ENSP00000379102.1:n.*76_*79del
ENST00000479543.2:n.1353_1356del
ENST00000642171.1:c.*183_*186del	ENSP00000495538.1:n.*183_*186del
ENST00000642448.1:n.1893_1896del
ENST00000642769.1:c.1041+26_1041+29del
ENST00000643000.1:c.*76_*79del	ENSP00000495164.1:n.*76_*79del
ENST00000643522.1:c.*76_*79del	ENSP00000496375.1:n.*76_*79del
ENST00000644050.1:c.*76_*79del	ENSP00000496123.1:n.*76_*79del
ENST00000644299.1:c.*76_*79del	ENSP00000494669.1:n.*76_*79del
ENST00000644459.1:c.*293_*296del	ENSP00000495861.1:n.*293_*296del
ENST00000644779.1:c.*76_*79del	ENSP00000494258.1:n.*76_*79del
ENST00000644868.1:c.1863_1866del	ENSP00000496760.1:n.1863_1866del
ENST00000645194.1:c.*76_*79del	ENSP00000496093.1:n.*76_*79del
ENST00000645303.1:c.*76_*79del	ENSP00000496667.1:n.*76_*79del
ENST00000645542.1:n.507_510del
ENST00000645634.1:c.*76_*79del	ENSP00000493945.1:n.*76_*79del
ENST00000646080.1:c.*76_*79del	ENSP00000494113.1:n.*76_*79del
ENST00000647076.1:c.516+26_516+29del
ENST00000647104.1:c.*76_*79del	ENSP00000494025.1:n.*76_*79del
ENST00000278379.7:c.*76_*79del	ENSP00000278379.3:n.*76_*79del
ENST00000395750.5:c.*76_*79del	ENSP00000379099.1:n.*76_*79del
ENST00000395753.5:c.*76_*79del	ENSP00000379102.1:n.*76_*79del
ENST00000464522.2:c.219+4709_219+4712del	ENSP00000435406.1:n.219+4709_219+4712del
NM_001195728.2:c.*76_*79del	NP_001182657.1:n.*76_*79del
NM_001252652.1:c.*76_*79del	NP_001239581.1:n.*76_*79del
NM_004171.3:c.*76_*79del	NP_004162.2:n.*76_*79del
XM_005253067.1:c.*76_*79del	XP_005253124.1:n.*76_*79del
XM_011520284.1:c.*76_*79del	XP_011518586.1:n.*76_*79del
XM_011520285.1:c.*76_*79del	XP_011518587.1:n.*76_*79del
XM_011520286.1:c.*76_*79del	XP_011518588.1:n.*76_*79del
XM_011520287.1:c.*76_*79del	XP_011518589.1:n.*76_*79del
XM_011520285.2:c.*76_*79del	XP_011518587.1:n.*76_*79del
XM_017018136.1:c.*76_*79del	XP_016873625.1:n.*76_*79del
XM_017018137.1:c.*76_*79del	XP_016873626.1:n.*76_*79del
XM_017018138.1:c.*76_*79del	XP_016873627.1:n.*76_*79del
XM_017018139.1:c.*76_*79del	XP_016873628.1:n.*76_*79del
NM_004171.4:c.*76_*79del MANE Select	NP_004162.2:n.*76_*79del
NM_001195728.3:c.*76_*79del	NP_001182657.1:n.*76_*79del
NM_001252652.2:c.*76_*79del	NP_001239581.1:n.*76_*79del