Canonical Allele Identifier: CA382896460
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025328A>T , CM000673.2:g.119025328A>T GRCh38
NC_000011.9:g.118896038A>T , CM000673.1:g.118896038A>T GRCh37
NC_000011.8:g.118401248A>T NCBI36
NG_013331.1:g.10578T>A , LRG_187:g.10578T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1196T>A (SLC37A4)
ENST00000697845.1:n.2185T>A (SLC37A4)
ENST00000697846.1:n.1558T>A (SLC37A4)
ENST00000697847.1:n.1269T>A (SLC37A4)
ENST00000697849.1:n.3662T>A (SLC37A4)
ENST00000697850.1:n.1853T>A (SLC37A4)
ENST00000697851.1:n.2824T>A (SLC37A4)
ENST00000638186.1:n.1290T>A (SLC37A4)
ENST00000638360.1:n.1122T>A (SLC37A4)
ENST00000638925.1:n.1255T>A (SLC37A4)
ENST00000650539.1:n.1458T>A (SLC37A4)
ENST00000330775.9:c.986T>A (SLC37A4) ENSP00000476242.2:p.Leu329His
ENST00000357590.9:c.1052T>A (SLC37A4) ENSP00000476176.2:p.Leu351His
ENST00000524428.5:n.1222T>A (SLC37A4)
ENST00000525039.5:n.1476T>A (SLC37A4)
ENST00000525102.5:n.1744T>A (SLC37A4)
ENST00000525372.5:n.1084T>A (SLC37A4)
ENST00000526275.5:n.1768T>A (SLC37A4)
ENST00000527992.5:n.1214T>A (SLC37A4)
ENST00000529510.5:n.674T>A (SLC37A4)
ENST00000530407.5:n.1136T>A (SLC37A4)
ENST00000532085.1:n.5004T>A (SLC37A4)
ENST00000533058.5:c.*279A>T (TRAPPC4) ENSP00000432920.1:n.*279A>T
ENST00000538950.5:c.767T>A (SLC37A4) ENSP00000475991.2:p.Leu256His
ENST00000545985.5:c.986T>A (SLC37A4) ENSP00000475241.2:p.Leu329His
NM_001164277.1:c.986T>A , LRG_187t1:c.986T>A (SLC37A4) NP_001157749.1:p.Leu329His
NM_001164278.1:c.1052T>A (SLC37A4) NP_001157750.1:p.Leu351His
NM_001164279.1:c.767T>A (SLC37A4) NP_001157751.1:p.Leu256His
NM_001164280.1:c.986T>A (SLC37A4) NP_001157752.1:p.Leu329His
NM_001467.5:c.986T>A (SLC37A4) NP_001458.1:p.Leu329His
NM_001164278.2:c.1052T>A (SLC37A4) NP_001157750.1:p.Leu351His
NM_001164279.2:c.767T>A (SLC37A4) NP_001157751.1:p.Leu256His
NM_001164280.2:c.986T>A (SLC37A4) NP_001157752.1:p.Leu329His
NM_001467.6:c.986T>A (SLC37A4) NP_001458.1:p.Leu329His
NM_001164277.2:c.986T>A (SLC37A4) MANE Select NP_001157749.1:p.Leu329His