Canonical Allele Identifier: CA2003748421

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025257C= , CM000673.2:g.119025257C=	GRCh38
NC_000011.9:g.118895967C= , CM000673.1:g.118895967C=	GRCh37
NC_000011.8:g.118401177C=	NCBI36
NG_013331.1:g.10649G= , LRG_187:g.10649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1267G= (SLC37A4)
ENST00000697845.1:n.2256G= (SLC37A4)
ENST00000697846.1:n.1629G= (SLC37A4)
ENST00000697847.1:n.1340G= (SLC37A4)
ENST00000697849.1:n.3733G= (SLC37A4)
ENST00000697850.1:n.1924G= (SLC37A4)
ENST00000697851.1:n.2895G= (SLC37A4)
ENST00000638186.1:n.1361G= (SLC37A4)
ENST00000638360.1:n.1193G= (SLC37A4)
ENST00000638925.1:n.1326G= (SLC37A4)
ENST00000650539.1:n.1529G= (SLC37A4)
ENST00000330775.9:c.1057G= (SLC37A4)	ENSP00000476242.2:p.Ala353=
ENST00000357590.9:c.1123G= (SLC37A4)	ENSP00000476176.2:p.Ala375=
ENST00000524428.5:n.1293G= (SLC37A4)
ENST00000525039.5:n.1547G= (SLC37A4)
ENST00000525102.5:n.1815G= (SLC37A4)
ENST00000525372.5:n.1155G= (SLC37A4)
ENST00000526275.5:n.1839G= (SLC37A4)
ENST00000527992.5:n.1285G= (SLC37A4)
ENST00000529510.5:n.745G= (SLC37A4)
ENST00000530407.5:n.1207G= (SLC37A4)
ENST00000532085.1:n.5075G= (SLC37A4)
ENST00000533058.5:c.*208C= (TRAPPC4)	ENSP00000432920.1:n.*208C=
ENST00000538950.5:c.838G= (SLC37A4)	ENSP00000475991.2:p.Ala280=
ENST00000545985.5:c.1057G= (SLC37A4)	ENSP00000475241.2:p.Ala353=
NM_001164277.1:c.1057G= , LRG_187t1:c.1057G= (SLC37A4)	NP_001157749.1:p.Ala353=
NM_001164278.1:c.1123G= (SLC37A4)	NP_001157750.1:p.Ala375=
NM_001164279.1:c.838G= (SLC37A4)	NP_001157751.1:p.Ala280=
NM_001164280.1:c.1057G= (SLC37A4)	NP_001157752.1:p.Ala353=
NM_001467.5:c.1057G= (SLC37A4)	NP_001458.1:p.Ala353=
NM_001164278.2:c.1123G= (SLC37A4)	NP_001157750.1:p.Ala375=
NM_001164279.2:c.838G= (SLC37A4)	NP_001157751.1:p.Ala280=
NM_001164280.2:c.1057G= (SLC37A4)	NP_001157752.1:p.Ala353=
NM_001467.6:c.1057G= (SLC37A4)	NP_001458.1:p.Ala353=
NM_001164277.2:c.1057G= (SLC37A4) MANE Select	NP_001157749.1:p.Ala353=