Canonical Allele Identifier: CA477367322
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118895950A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025240A>C , CM000673.2:g.119025240A>C GRCh38
NC_000011.9:g.118895950A>C , CM000673.1:g.118895950A>C GRCh37
NC_000011.8:g.118401160A>C NCBI36
NG_013331.1:g.10666T>G , LRG_187:g.10666T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1284T>G (SLC37A4)
ENST00000697845.1:n.2273T>G (SLC37A4)
ENST00000697846.1:n.1646T>G (SLC37A4)
ENST00000697847.1:n.1357T>G (SLC37A4)
ENST00000697849.1:n.3750T>G (SLC37A4)
ENST00000697850.1:n.1941T>G (SLC37A4)
ENST00000697851.1:n.2912T>G (SLC37A4)
ENST00000638186.1:n.1378T>G (SLC37A4)
ENST00000638360.1:n.1210T>G (SLC37A4)
ENST00000638925.1:n.1343T>G (SLC37A4)
ENST00000650539.1:n.1546T>G (SLC37A4)
ENST00000330775.9:c.1074T>G (SLC37A4) ENSP00000476242.2:p.Pro358=
ENST00000357590.9:c.1140T>G (SLC37A4) ENSP00000476176.2:p.Pro380=
ENST00000524428.5:n.1310T>G (SLC37A4)
ENST00000525039.5:n.1564T>G (SLC37A4)
ENST00000525102.5:n.1832T>G (SLC37A4)
ENST00000525372.5:n.1172T>G (SLC37A4)
ENST00000526275.5:n.1856T>G (SLC37A4)
ENST00000527992.5:n.1302T>G (SLC37A4)
ENST00000529510.5:n.762T>G (SLC37A4)
ENST00000530407.5:n.1224T>G (SLC37A4)
ENST00000532085.1:n.5092T>G (SLC37A4)
ENST00000533058.5:c.*191A>C (TRAPPC4) ENSP00000432920.1:n.*191A>C
ENST00000538950.5:c.855T>G (SLC37A4) ENSP00000475991.2:p.Pro285=
ENST00000545985.5:c.1074T>G (SLC37A4) ENSP00000475241.2:p.Pro358=
NM_001164277.1:c.1074T>G , LRG_187t1:c.1074T>G (SLC37A4) NP_001157749.1:p.Pro358=
NM_001164278.1:c.1140T>G (SLC37A4) NP_001157750.1:p.Pro380=
NM_001164279.1:c.855T>G (SLC37A4) NP_001157751.1:p.Pro285=
NM_001164280.1:c.1074T>G (SLC37A4) NP_001157752.1:p.Pro358=
NM_001467.5:c.1074T>G (SLC37A4) NP_001458.1:p.Pro358=
NM_001164278.2:c.1140T>G (SLC37A4) NP_001157750.1:p.Pro380=
NM_001164279.2:c.855T>G (SLC37A4) NP_001157751.1:p.Pro285=
NM_001164280.2:c.1074T>G (SLC37A4) NP_001157752.1:p.Pro358=
NM_001467.6:c.1074T>G (SLC37A4) NP_001458.1:p.Pro358=
NM_001164277.2:c.1074T>G (SLC37A4) MANE Select NP_001157749.1:p.Pro358=