Canonical Allele Identifier: CA2003749698

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943615775

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027725del , CM000673.2:g.119027725del	GRCh38
NC_000011.9:g.118898435del , CM000673.1:g.118898435del	GRCh37
NC_000011.8:g.118403645del	NCBI36
NG_013331.1:g.8181del , LRG_187:g.8181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.758del
ENST00000697845.1:n.682del
ENST00000697846.1:n.758del
ENST00000697847.1:n.758del
ENST00000697848.1:n.758del
ENST00000697849.1:n.1797del
ENST00000697850.1:n.758del
ENST00000697851.1:n.2118del
ENST00000638186.1:n.832del
ENST00000638360.1:n.664del
ENST00000638925.1:n.765del
ENST00000650539.1:n.934del
ENST00000330775.9:c.529-1del	ENSP00000476242.2:n.529-1del
ENST00000357590.9:c.529-1del	ENSP00000476176.2:n.529-1del
ENST00000524428.5:n.850del
ENST00000525039.5:n.952del
ENST00000525102.5:n.1286del
ENST00000525372.5:n.529del
ENST00000526275.5:n.1310del
ENST00000526626.6:n.491del
ENST00000527992.5:n.756del
ENST00000529510.5:n.399+469del
ENST00000530407.5:n.678del
ENST00000532085.1:n.3139del
ENST00000532888.6:n.824del
ENST00000538950.5:c.310-1del	ENSP00000475991.2:n.310-1del
ENST00000545985.5:c.529-1del	ENSP00000475241.2:n.529-1del
NM_001164277.1:c.528del , LRG_187t1:c.528del	NP_001157749.1:p.Cys176TrpfsTer?
NM_001164278.1:c.528del	NP_001157750.1:p.Cys176TrpfsTer?
NM_001164279.1:c.309del	NP_001157751.1:p.Cys103TrpfsTer?
NM_001164280.1:c.528del	NP_001157752.1:p.Cys176TrpfsTer?
NM_001467.5:c.528del	NP_001458.1:p.Cys176TrpfsTer?
NM_001164278.2:c.528del	NP_001157750.1:p.Cys176TrpfsTer?
NM_001164279.2:c.309del	NP_001157751.1:p.Cys103TrpfsTer?
NM_001164280.2:c.528del	NP_001157752.1:p.Cys176TrpfsTer?
NM_001467.6:c.528del	NP_001458.1:p.Cys176TrpfsTer?
NM_001164277.2:c.528del MANE Select	NP_001157749.1:p.Cys176TrpfsTer?