Canonical Allele Identifier: CA117427516

Gene: SLC1A3

Linked Data

• dbSNP Id: rs747172655
• gnomAD v3: 5-36687651-C-T
• gnomAD v4: 5-36687651-C-T
• MyVariant Identifiers: chr5:g.36687753C>T (hg19) ; chr5:g.36687651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36687651C>T , CM000667.2:g.36687651C>T	GRCh38
NC_000005.9:g.36687753C>T , CM000667.1:g.36687753C>T	GRCh37
NC_000005.8:g.36723510C>T	NCBI36
NG_015890.1:g.86297C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265113.9:c.*1382C>T MANE Select	ENSP00000265113.4:n.*1382C>T
ENST00000381918.4:c.*1382C>T	ENSP00000371343.4:n.*1382C>T
ENST00000612708.5:c.*1382C>T	ENSP00000483657.1:n.*1382C>T
ENST00000613445.5:c.*1382C>T	ENSP00000477672.1:n.*1382C>T
ENST00000624112.2:n.6004C>T
ENST00000679784.1:c.*2923C>T	ENSP00000506030.1:n.*2923C>T
ENST00000679852.1:c.1821C>T
ENST00000679958.1:c.*1504C>T	ENSP00000505246.1:n.*1504C>T
ENST00000679983.1:c.*1382C>T	ENSP00000505238.1:n.*1382C>T
ENST00000679992.1:c.*1382C>T	ENSP00000506585.1:n.*1382C>T
ENST00000680048.1:c.*3504C>T	ENSP00000505296.1:n.*3504C>T
ENST00000680125.1:c.*1382C>T	ENSP00000506424.1:n.*1382C>T
ENST00000680232.1:c.*1382C>T	ENSP00000506207.1:n.*1382C>T
ENST00000680318.1:c.*1382C>T	ENSP00000505057.1:n.*1382C>T
ENST00000680568.1:n.2239C>T
ENST00000680655.1:c.*2723C>T	ENSP00000506436.1:n.*2723C>T
ENST00000680876.1:n.6192C>T
ENST00000680878.1:n.6057C>T
ENST00000681633.1:n.5819C>T
ENST00000681926.1:c.*1382C>T	ENSP00000505850.1:n.*1382C>T
ENST00000265113.8:c.*1382C>T	ENSP00000265113.4:n.*1382C>T
ENST00000381918.3:c.*1382C>T	ENSP00000371343.3:n.*1382C>T
ENST00000612708.4:c.*1382C>T	ENSP00000483657.1:n.*1382C>T
ENST00000613445.4:c.*1382C>T	ENSP00000477672.1:n.*1382C>T
NM_001166695.2:c.*1382C>T	NP_001160167.1:n.*1382C>T
NM_001289939.1:c.*1382C>T	NP_001276868.1:n.*1382C>T
NM_001289940.1:c.*1382C>T	NP_001276869.1:n.*1382C>T
NM_004172.4:c.*1382C>T	NP_004163.3:n.*1382C>T
XM_005248342.1:c.*1382C>T	XP_005248399.1:n.*1382C>T
XM_011514084.1:c.*1382C>T	XP_011512386.1:n.*1382C>T
XM_005248342.3:c.*1382C>T	XP_005248399.1:n.*1382C>T
XM_011514084.2:c.*1382C>T	XP_011512386.1:n.*1382C>T
XM_024446181.1:c.*1382C>T	XP_024301949.1:n.*1382C>T
XM_024446182.1:c.*1382C>T	XP_024301950.1:n.*1382C>T
NM_004172.5:c.*1382C>T MANE Select	NP_004163.3:n.*1382C>T
NM_001166695.3:c.*1382C>T	NP_001160167.1:n.*1382C>T
NM_001289939.2:c.*1382C>T	NP_001276868.1:n.*1382C>T
NM_001289940.2:c.*1382C>T	NP_001276869.1:n.*1382C>T