Canonical Allele Identifier: CA382896378
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1319691487

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025316A>C , CM000673.2:g.119025316A>C GRCh38
NC_000011.9:g.118896026A>C , CM000673.1:g.118896026A>C GRCh37
NC_000011.8:g.118401236A>C NCBI36
NG_013331.1:g.10590T>G , LRG_187:g.10590T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1208T>G (SLC37A4)
ENST00000697845.1:n.2197T>G (SLC37A4)
ENST00000697846.1:n.1570T>G (SLC37A4)
ENST00000697847.1:n.1281T>G (SLC37A4)
ENST00000697849.1:n.3674T>G (SLC37A4)
ENST00000697850.1:n.1865T>G (SLC37A4)
ENST00000697851.1:n.2836T>G (SLC37A4)
ENST00000638186.1:n.1302T>G (SLC37A4)
ENST00000638360.1:n.1134T>G (SLC37A4)
ENST00000638925.1:n.1267T>G (SLC37A4)
ENST00000650539.1:n.1470T>G (SLC37A4)
ENST00000330775.9:c.998T>G (SLC37A4) ENSP00000476242.2:p.Val333Gly
ENST00000357590.9:c.1064T>G (SLC37A4) ENSP00000476176.2:p.Val355Gly
ENST00000524428.5:n.1234T>G (SLC37A4)
ENST00000525039.5:n.1488T>G (SLC37A4)
ENST00000525102.5:n.1756T>G (SLC37A4)
ENST00000525372.5:n.1096T>G (SLC37A4)
ENST00000526275.5:n.1780T>G (SLC37A4)
ENST00000527992.5:n.1226T>G (SLC37A4)
ENST00000529510.5:n.686T>G (SLC37A4)
ENST00000530407.5:n.1148T>G (SLC37A4)
ENST00000532085.1:n.5016T>G (SLC37A4)
ENST00000533058.5:c.*267A>C (TRAPPC4) ENSP00000432920.1:n.*267A>C
ENST00000538950.5:c.779T>G (SLC37A4) ENSP00000475991.2:p.Val260Gly
ENST00000545985.5:c.998T>G (SLC37A4) ENSP00000475241.2:p.Val333Gly
NM_001164277.1:c.998T>G , LRG_187t1:c.998T>G (SLC37A4) NP_001157749.1:p.Val333Gly
NM_001164278.1:c.1064T>G (SLC37A4) NP_001157750.1:p.Val355Gly
NM_001164279.1:c.779T>G (SLC37A4) NP_001157751.1:p.Val260Gly
NM_001164280.1:c.998T>G (SLC37A4) NP_001157752.1:p.Val333Gly
NM_001467.5:c.998T>G (SLC37A4) NP_001458.1:p.Val333Gly
NM_001164278.2:c.1064T>G (SLC37A4) NP_001157750.1:p.Val355Gly
NM_001164279.2:c.779T>G (SLC37A4) NP_001157751.1:p.Val260Gly
NM_001164280.2:c.998T>G (SLC37A4) NP_001157752.1:p.Val333Gly
NM_001467.6:c.998T>G (SLC37A4) NP_001458.1:p.Val333Gly
NM_001164277.2:c.998T>G (SLC37A4) MANE Select NP_001157749.1:p.Val333Gly