Canonical Allele Identifier: CA2003748454
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025314A= , CM000673.2:g.119025314A= GRCh38
NC_000011.9:g.118896024A= , CM000673.1:g.118896024A= GRCh37
NC_000011.8:g.118401234A= NCBI36
NG_013331.1:g.10592T= , LRG_187:g.10592T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1210T= (SLC37A4)
ENST00000697845.1:n.2199T= (SLC37A4)
ENST00000697846.1:n.1572T= (SLC37A4)
ENST00000697847.1:n.1283T= (SLC37A4)
ENST00000697849.1:n.3676T= (SLC37A4)
ENST00000697850.1:n.1867T= (SLC37A4)
ENST00000697851.1:n.2838T= (SLC37A4)
ENST00000638186.1:n.1304T= (SLC37A4)
ENST00000638360.1:n.1136T= (SLC37A4)
ENST00000638925.1:n.1269T= (SLC37A4)
ENST00000650539.1:n.1472T= (SLC37A4)
ENST00000330775.9:c.1000T= (SLC37A4) ENSP00000476242.2:p.Leu334=
ENST00000357590.9:c.1066T= (SLC37A4) ENSP00000476176.2:p.Leu356=
ENST00000524428.5:n.1236T= (SLC37A4)
ENST00000525039.5:n.1490T= (SLC37A4)
ENST00000525102.5:n.1758T= (SLC37A4)
ENST00000525372.5:n.1098T= (SLC37A4)
ENST00000526275.5:n.1782T= (SLC37A4)
ENST00000527992.5:n.1228T= (SLC37A4)
ENST00000529510.5:n.688T= (SLC37A4)
ENST00000530407.5:n.1150T= (SLC37A4)
ENST00000532085.1:n.5018T= (SLC37A4)
ENST00000533058.5:c.*265A= (TRAPPC4) ENSP00000432920.1:n.*265A=
ENST00000538950.5:c.781T= (SLC37A4) ENSP00000475991.2:p.Leu261=
ENST00000545985.5:c.1000T= (SLC37A4) ENSP00000475241.2:p.Leu334=
NM_001164277.1:c.1000T= , LRG_187t1:c.1000T= (SLC37A4) NP_001157749.1:p.Leu334=
NM_001164278.1:c.1066T= (SLC37A4) NP_001157750.1:p.Leu356=
NM_001164279.1:c.781T= (SLC37A4) NP_001157751.1:p.Leu261=
NM_001164280.1:c.1000T= (SLC37A4) NP_001157752.1:p.Leu334=
NM_001467.5:c.1000T= (SLC37A4) NP_001458.1:p.Leu334=
NM_001164278.2:c.1066T= (SLC37A4) NP_001157750.1:p.Leu356=
NM_001164279.2:c.781T= (SLC37A4) NP_001157751.1:p.Leu261=
NM_001164280.2:c.1000T= (SLC37A4) NP_001157752.1:p.Leu334=
NM_001467.6:c.1000T= (SLC37A4) NP_001458.1:p.Leu334=
NM_001164277.2:c.1000T= (SLC37A4) MANE Select NP_001157749.1:p.Leu334=