Canonical Allele Identifier: CA2003748388
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025196G= , CM000673.2:g.119025196G= GRCh38
NC_000011.9:g.118895906G= , CM000673.1:g.118895906G= GRCh37
NC_000011.8:g.118401116G= NCBI36
NG_013331.1:g.10710C= , LRG_187:g.10710C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1328C= (SLC37A4)
ENST00000697845.1:n.2317C= (SLC37A4)
ENST00000697846.1:n.1690C= (SLC37A4)
ENST00000697847.1:n.1401C= (SLC37A4)
ENST00000697849.1:n.3794C= (SLC37A4)
ENST00000697850.1:n.1985C= (SLC37A4)
ENST00000697851.1:n.2956C= (SLC37A4)
ENST00000638186.1:n.1422C= (SLC37A4)
ENST00000638360.1:n.1254C= (SLC37A4)
ENST00000638925.1:n.1387C= (SLC37A4)
ENST00000650539.1:n.1590C= (SLC37A4)
ENST00000330775.9:c.1118C= (SLC37A4) ENSP00000476242.2:p.Ala373=
ENST00000357590.9:c.1184C= (SLC37A4) ENSP00000476176.2:p.Ala395=
ENST00000524428.5:n.1354C= (SLC37A4)
ENST00000525039.5:n.1608C= (SLC37A4)
ENST00000525102.5:n.1876C= (SLC37A4)
ENST00000525372.5:n.1216C= (SLC37A4)
ENST00000526275.5:n.1900C= (SLC37A4)
ENST00000527992.5:n.1346C= (SLC37A4)
ENST00000529510.5:n.806C= (SLC37A4)
ENST00000530407.5:n.1268C= (SLC37A4)
ENST00000532085.1:n.5136C= (SLC37A4)
ENST00000533058.5:c.*147G= (TRAPPC4) ENSP00000432920.1:n.*147G=
ENST00000538950.5:c.899C= (SLC37A4) ENSP00000475991.2:p.Ala300=
ENST00000545985.5:c.1118C= (SLC37A4) ENSP00000475241.2:p.Ala373=
NM_001164277.1:c.1118C= , LRG_187t1:c.1118C= (SLC37A4) NP_001157749.1:p.Ala373=
NM_001164278.1:c.1184C= (SLC37A4) NP_001157750.1:p.Ala395=
NM_001164279.1:c.899C= (SLC37A4) NP_001157751.1:p.Ala300=
NM_001164280.1:c.1118C= (SLC37A4) NP_001157752.1:p.Ala373=
NM_001467.5:c.1118C= (SLC37A4) NP_001458.1:p.Ala373=
NM_001164278.2:c.1184C= (SLC37A4) NP_001157750.1:p.Ala395=
NM_001164279.2:c.899C= (SLC37A4) NP_001157751.1:p.Ala300=
NM_001164280.2:c.1118C= (SLC37A4) NP_001157752.1:p.Ala373=
NM_001467.6:c.1118C= (SLC37A4) NP_001458.1:p.Ala373=
NM_001164277.2:c.1118C= (SLC37A4) MANE Select NP_001157749.1:p.Ala373=