Canonical Allele Identifier: CA382896413
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025322A>G , CM000673.2:g.119025322A>G GRCh38
NC_000011.9:g.118896032A>G , CM000673.1:g.118896032A>G GRCh37
NC_000011.8:g.118401242A>G NCBI36
NG_013331.1:g.10584T>C , LRG_187:g.10584T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1202T>C (SLC37A4)
ENST00000697845.1:n.2191T>C (SLC37A4)
ENST00000697846.1:n.1564T>C (SLC37A4)
ENST00000697847.1:n.1275T>C (SLC37A4)
ENST00000697849.1:n.3668T>C (SLC37A4)
ENST00000697850.1:n.1859T>C (SLC37A4)
ENST00000697851.1:n.2830T>C (SLC37A4)
ENST00000638186.1:n.1296T>C (SLC37A4)
ENST00000638360.1:n.1128T>C (SLC37A4)
ENST00000638925.1:n.1261T>C (SLC37A4)
ENST00000650539.1:n.1464T>C (SLC37A4)
ENST00000330775.9:c.992T>C (SLC37A4) ENSP00000476242.2:p.Ile331Thr
ENST00000357590.9:c.1058T>C (SLC37A4) ENSP00000476176.2:p.Ile353Thr
ENST00000524428.5:n.1228T>C (SLC37A4)
ENST00000525039.5:n.1482T>C (SLC37A4)
ENST00000525102.5:n.1750T>C (SLC37A4)
ENST00000525372.5:n.1090T>C (SLC37A4)
ENST00000526275.5:n.1774T>C (SLC37A4)
ENST00000527992.5:n.1220T>C (SLC37A4)
ENST00000529510.5:n.680T>C (SLC37A4)
ENST00000530407.5:n.1142T>C (SLC37A4)
ENST00000532085.1:n.5010T>C (SLC37A4)
ENST00000533058.5:c.*273A>G (TRAPPC4) ENSP00000432920.1:n.*273A>G
ENST00000538950.5:c.773T>C (SLC37A4) ENSP00000475991.2:p.Ile258Thr
ENST00000545985.5:c.992T>C (SLC37A4) ENSP00000475241.2:p.Ile331Thr
NM_001164277.1:c.992T>C , LRG_187t1:c.992T>C (SLC37A4) NP_001157749.1:p.Ile331Thr
NM_001164278.1:c.1058T>C (SLC37A4) NP_001157750.1:p.Ile353Thr
NM_001164279.1:c.773T>C (SLC37A4) NP_001157751.1:p.Ile258Thr
NM_001164280.1:c.992T>C (SLC37A4) NP_001157752.1:p.Ile331Thr
NM_001467.5:c.992T>C (SLC37A4) NP_001458.1:p.Ile331Thr
NM_001164278.2:c.1058T>C (SLC37A4) NP_001157750.1:p.Ile353Thr
NM_001164279.2:c.773T>C (SLC37A4) NP_001157751.1:p.Ile258Thr
NM_001164280.2:c.992T>C (SLC37A4) NP_001157752.1:p.Ile331Thr
NM_001467.6:c.992T>C (SLC37A4) NP_001458.1:p.Ile331Thr
NM_001164277.2:c.992T>C (SLC37A4) MANE Select NP_001157749.1:p.Ile331Thr