Canonical Allele Identifier: CA2003748311
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025048G= , CM000673.2:g.119025048G= GRCh38
NC_000011.9:g.118895758G= , CM000673.1:g.118895758G= GRCh37
NC_000011.8:g.118400968G= NCBI36
NG_013331.1:g.10858C= , LRG_187:g.10858C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1362C= (SLC37A4)
ENST00000697845.1:n.2351C= (SLC37A4)
ENST00000697846.1:n.1724C= (SLC37A4)
ENST00000697847.1:n.1435C= (SLC37A4)
ENST00000697849.1:n.3828C= (SLC37A4)
ENST00000697850.1:n.2019C= (SLC37A4)
ENST00000697851.1:n.2990C= (SLC37A4)
ENST00000638186.1:n.1456C= (SLC37A4)
ENST00000638360.1:n.1288C= (SLC37A4)
ENST00000638925.1:n.1421C= (SLC37A4)
ENST00000650539.1:n.1624C= (SLC37A4)
ENST00000330775.9:c.1152C= (SLC37A4) ENSP00000476242.2:p.Phe384=
ENST00000357590.9:c.1218C= (SLC37A4) ENSP00000476176.2:p.Phe406=
ENST00000524428.5:n.1388C= (SLC37A4)
ENST00000525039.5:n.1642C= (SLC37A4)
ENST00000525102.5:n.1910C= (SLC37A4)
ENST00000525372.5:n.1250C= (SLC37A4)
ENST00000526275.5:n.1934C= (SLC37A4)
ENST00000527992.5:n.1380C= (SLC37A4)
ENST00000530407.5:n.1302C= (SLC37A4)
ENST00000532085.1:n.5170C= (SLC37A4)
ENST00000533058.5:c.773G= (TRAPPC4) ENSP00000432920.1:p.Ter258=
ENST00000538950.5:c.933C= (SLC37A4) ENSP00000475991.2:p.Phe311=
ENST00000545985.5:c.1152C= (SLC37A4) ENSP00000475241.2:p.Phe384=
NM_001164277.1:c.1152C= , LRG_187t1:c.1152C= (SLC37A4) NP_001157749.1:p.Phe384=
NM_001164278.1:c.1218C= (SLC37A4) NP_001157750.1:p.Phe406=
NM_001164279.1:c.933C= (SLC37A4) NP_001157751.1:p.Phe311=
NM_001164280.1:c.1152C= (SLC37A4) NP_001157752.1:p.Phe384=
NM_001467.5:c.1152C= (SLC37A4) NP_001458.1:p.Phe384=
NM_001164278.2:c.1218C= (SLC37A4) NP_001157750.1:p.Phe406=
NM_001164279.2:c.933C= (SLC37A4) NP_001157751.1:p.Phe311=
NM_001164280.2:c.1152C= (SLC37A4) NP_001157752.1:p.Phe384=
NM_001467.6:c.1152C= (SLC37A4) NP_001458.1:p.Phe384=
NM_001164277.2:c.1152C= (SLC37A4) MANE Select NP_001157749.1:p.Phe384=