Canonical Allele Identifier: CA2003748298
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025029A= , CM000673.2:g.119025029A= GRCh38
NC_000011.9:g.118895739A= , CM000673.1:g.118895739A= GRCh37
NC_000011.8:g.118400949A= NCBI36
NG_013331.1:g.10877T= , LRG_187:g.10877T=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1381T= (SLC37A4)
ENST00000697845.1:n.2370T= (SLC37A4)
ENST00000697846.1:n.1743T= (SLC37A4)
ENST00000697847.1:n.1454T= (SLC37A4)
ENST00000697849.1:n.3847T= (SLC37A4)
ENST00000697850.1:n.2038T= (SLC37A4)
ENST00000697851.1:n.3009T= (SLC37A4)
ENST00000638186.1:n.1475T= (SLC37A4)
ENST00000638360.1:n.1307T= (SLC37A4)
ENST00000638925.1:n.1440T= (SLC37A4)
ENST00000650539.1:n.1643T= (SLC37A4)
ENST00000330775.9:c.1171T= (SLC37A4) ENSP00000476242.2:p.Tyr391=
ENST00000357590.9:c.1237T= (SLC37A4) ENSP00000476176.2:p.Tyr413=
ENST00000524428.5:n.1407T= (SLC37A4)
ENST00000525039.5:n.1661T= (SLC37A4)
ENST00000525102.5:n.1929T= (SLC37A4)
ENST00000525372.5:n.1269T= (SLC37A4)
ENST00000526275.5:n.1953T= (SLC37A4)
ENST00000527992.5:n.1399T= (SLC37A4)
ENST00000530407.5:n.1321T= (SLC37A4)
ENST00000532085.1:n.5189T= (SLC37A4)
ENST00000533058.5:c.754A= (TRAPPC4) ENSP00000432920.1:p.Ser252=
ENST00000538950.5:c.952T= (SLC37A4) ENSP00000475991.2:p.Tyr318=
ENST00000545985.5:c.1171T= (SLC37A4) ENSP00000475241.2:p.Tyr391=
NM_001164277.1:c.1171T= , LRG_187t1:c.1171T= (SLC37A4) NP_001157749.1:p.Tyr391=
NM_001164278.1:c.1237T= (SLC37A4) NP_001157750.1:p.Tyr413=
NM_001164279.1:c.952T= (SLC37A4) NP_001157751.1:p.Tyr318=
NM_001164280.1:c.1171T= (SLC37A4) NP_001157752.1:p.Tyr391=
NM_001467.5:c.1171T= (SLC37A4) NP_001458.1:p.Tyr391=
NM_001164278.2:c.1237T= (SLC37A4) NP_001157750.1:p.Tyr413=
NM_001164279.2:c.952T= (SLC37A4) NP_001157751.1:p.Tyr318=
NM_001164280.2:c.1171T= (SLC37A4) NP_001157752.1:p.Tyr391=
NM_001467.6:c.1171T= (SLC37A4) NP_001458.1:p.Tyr391=
NM_001164277.2:c.1171T= (SLC37A4) MANE Select NP_001157749.1:p.Tyr391=