Canonical Allele Identifier: CA2003748134
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024729G= , CM000673.2:g.119024729G= GRCh38
NC_000011.9:g.118895439G= , CM000673.1:g.118895439G= GRCh37
NC_000011.8:g.118400649G= NCBI36
NG_013331.1:g.11177C= , LRG_187:g.11177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1681C= (SLC37A4)
ENST00000697845.1:n.2670C= (SLC37A4)
ENST00000697846.1:n.2043C= (SLC37A4)
ENST00000697847.1:n.1754C= (SLC37A4)
ENST00000697849.1:n.4147C= (SLC37A4)
ENST00000697850.1:n.2338C= (SLC37A4)
ENST00000697851.1:n.3309C= (SLC37A4)
ENST00000638186.1:n.1775C= (SLC37A4)
ENST00000638360.1:n.1607C= (SLC37A4)
ENST00000638925.1:n.1740C= (SLC37A4)
ENST00000650539.1:n.1943C= (SLC37A4)
ENST00000330775.9:c.*181C= (SLC37A4) ENSP00000476242.2:n.*181C=
ENST00000357590.9:c.*181C= (SLC37A4) ENSP00000476176.2:n.*181C=
ENST00000525102.5:n.2229C= (SLC37A4)
ENST00000526275.5:n.2253C= (SLC37A4)
ENST00000527992.5:n.1699C= (SLC37A4)
ENST00000532085.1:n.5489C= (SLC37A4)
ENST00000533058.5:c.582-128G= (TRAPPC4) ENSP00000432920.1:n.582-128G=
ENST00000538950.5:c.*181C= (SLC37A4) ENSP00000475991.2:n.*181C=
ENST00000545985.5:c.*181C= (SLC37A4) ENSP00000475241.2:n.*181C=
NM_001164277.1:c.*181C= , LRG_187t1:c.*181C= (SLC37A4) NP_001157749.1:n.*181C=
NM_001164278.1:c.*181C= (SLC37A4) NP_001157750.1:n.*181C=
NM_001164279.1:c.*181C= (SLC37A4) NP_001157751.1:n.*181C=
NM_001164280.1:c.*181C= (SLC37A4) NP_001157752.1:n.*181C=
NM_001467.5:c.*181C= (SLC37A4) NP_001458.1:n.*181C=
NM_001164278.2:c.*181C= (SLC37A4) NP_001157750.1:n.*181C=
NM_001164279.2:c.*181C= (SLC37A4) NP_001157751.1:n.*181C=
NM_001164280.2:c.*181C= (SLC37A4) NP_001157752.1:n.*181C=
NM_001467.6:c.*181C= (SLC37A4) NP_001458.1:n.*181C=
NM_001164277.2:c.*181C= (SLC37A4) MANE Select NP_001157749.1:n.*181C=