Canonical Allele Identifier: CA382896332
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025308C>T , CM000673.2:g.119025308C>T GRCh38
NC_000011.9:g.118896018C>T , CM000673.1:g.118896018C>T GRCh37
NC_000011.8:g.118401228C>T NCBI36
NG_013331.1:g.10598G>A , LRG_187:g.10598G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1216G>A (SLC37A4)
ENST00000697845.1:n.2205G>A (SLC37A4)
ENST00000697846.1:n.1578G>A (SLC37A4)
ENST00000697847.1:n.1289G>A (SLC37A4)
ENST00000697849.1:n.3682G>A (SLC37A4)
ENST00000697850.1:n.1873G>A (SLC37A4)
ENST00000697851.1:n.2844G>A (SLC37A4)
ENST00000638186.1:n.1310G>A (SLC37A4)
ENST00000638360.1:n.1142G>A (SLC37A4)
ENST00000638925.1:n.1275G>A (SLC37A4)
ENST00000650539.1:n.1478G>A (SLC37A4)
ENST00000330775.9:c.1006G>A (SLC37A4) ENSP00000476242.2:p.Ala336Thr
ENST00000357590.9:c.1072G>A (SLC37A4) ENSP00000476176.2:p.Ala358Thr
ENST00000524428.5:n.1242G>A (SLC37A4)
ENST00000525039.5:n.1496G>A (SLC37A4)
ENST00000525102.5:n.1764G>A (SLC37A4)
ENST00000525372.5:n.1104G>A (SLC37A4)
ENST00000526275.5:n.1788G>A (SLC37A4)
ENST00000527992.5:n.1234G>A (SLC37A4)
ENST00000529510.5:n.694G>A (SLC37A4)
ENST00000530407.5:n.1156G>A (SLC37A4)
ENST00000532085.1:n.5024G>A (SLC37A4)
ENST00000533058.5:c.*259C>T (TRAPPC4) ENSP00000432920.1:n.*259C>T
ENST00000538950.5:c.787G>A (SLC37A4) ENSP00000475991.2:p.Ala263Thr
ENST00000545985.5:c.1006G>A (SLC37A4) ENSP00000475241.2:p.Ala336Thr
NM_001164277.1:c.1006G>A , LRG_187t1:c.1006G>A (SLC37A4) NP_001157749.1:p.Ala336Thr
NM_001164278.1:c.1072G>A (SLC37A4) NP_001157750.1:p.Ala358Thr
NM_001164279.1:c.787G>A (SLC37A4) NP_001157751.1:p.Ala263Thr
NM_001164280.1:c.1006G>A (SLC37A4) NP_001157752.1:p.Ala336Thr
NM_001467.5:c.1006G>A (SLC37A4) NP_001458.1:p.Ala336Thr
NM_001164278.2:c.1072G>A (SLC37A4) NP_001157750.1:p.Ala358Thr
NM_001164279.2:c.787G>A (SLC37A4) NP_001157751.1:p.Ala263Thr
NM_001164280.2:c.1006G>A (SLC37A4) NP_001157752.1:p.Ala336Thr
NM_001467.6:c.1006G>A (SLC37A4) NP_001458.1:p.Ala336Thr
NM_001164277.2:c.1006G>A (SLC37A4) MANE Select NP_001157749.1:p.Ala336Thr