Canonical Allele Identifier: CA477367283
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118895932G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025222G>C , CM000673.2:g.119025222G>C GRCh38
NC_000011.9:g.118895932G>C , CM000673.1:g.118895932G>C GRCh37
NC_000011.8:g.118401142G>C NCBI36
NG_013331.1:g.10684C>G , LRG_187:g.10684C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1302C>G (SLC37A4)
ENST00000697845.1:n.2291C>G (SLC37A4)
ENST00000697846.1:n.1664C>G (SLC37A4)
ENST00000697847.1:n.1375C>G (SLC37A4)
ENST00000697849.1:n.3768C>G (SLC37A4)
ENST00000697850.1:n.1959C>G (SLC37A4)
ENST00000697851.1:n.2930C>G (SLC37A4)
ENST00000638186.1:n.1396C>G (SLC37A4)
ENST00000638360.1:n.1228C>G (SLC37A4)
ENST00000638925.1:n.1361C>G (SLC37A4)
ENST00000650539.1:n.1564C>G (SLC37A4)
ENST00000330775.9:c.1092C>G (SLC37A4) ENSP00000476242.2:p.Thr364=
ENST00000357590.9:c.1158C>G (SLC37A4) ENSP00000476176.2:p.Thr386=
ENST00000524428.5:n.1328C>G (SLC37A4)
ENST00000525039.5:n.1582C>G (SLC37A4)
ENST00000525102.5:n.1850C>G (SLC37A4)
ENST00000525372.5:n.1190C>G (SLC37A4)
ENST00000526275.5:n.1874C>G (SLC37A4)
ENST00000527992.5:n.1320C>G (SLC37A4)
ENST00000529510.5:n.780C>G (SLC37A4)
ENST00000530407.5:n.1242C>G (SLC37A4)
ENST00000532085.1:n.5110C>G (SLC37A4)
ENST00000533058.5:c.*173G>C (TRAPPC4) ENSP00000432920.1:n.*173G>C
ENST00000538950.5:c.873C>G (SLC37A4) ENSP00000475991.2:p.Thr291=
ENST00000545985.5:c.1092C>G (SLC37A4) ENSP00000475241.2:p.Thr364=
NM_001164277.1:c.1092C>G , LRG_187t1:c.1092C>G (SLC37A4) NP_001157749.1:p.Thr364=
NM_001164278.1:c.1158C>G (SLC37A4) NP_001157750.1:p.Thr386=
NM_001164279.1:c.873C>G (SLC37A4) NP_001157751.1:p.Thr291=
NM_001164280.1:c.1092C>G (SLC37A4) NP_001157752.1:p.Thr364=
NM_001467.5:c.1092C>G (SLC37A4) NP_001458.1:p.Thr364=
NM_001164278.2:c.1158C>G (SLC37A4) NP_001157750.1:p.Thr386=
NM_001164279.2:c.873C>G (SLC37A4) NP_001157751.1:p.Thr291=
NM_001164280.2:c.1092C>G (SLC37A4) NP_001157752.1:p.Thr364=
NM_001467.6:c.1092C>G (SLC37A4) NP_001458.1:p.Thr364=
NM_001164277.2:c.1092C>G (SLC37A4) MANE Select NP_001157749.1:p.Thr364=