Canonical Allele Identifier: CA382895317
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025211A>C , CM000673.2:g.119025211A>C GRCh38
NC_000011.9:g.118895921A>C , CM000673.1:g.118895921A>C GRCh37
NC_000011.8:g.118401131A>C NCBI36
NG_013331.1:g.10695T>G , LRG_187:g.10695T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1313T>G (SLC37A4)
ENST00000697845.1:n.2302T>G (SLC37A4)
ENST00000697846.1:n.1675T>G (SLC37A4)
ENST00000697847.1:n.1386T>G (SLC37A4)
ENST00000697849.1:n.3779T>G (SLC37A4)
ENST00000697850.1:n.1970T>G (SLC37A4)
ENST00000697851.1:n.2941T>G (SLC37A4)
ENST00000638186.1:n.1407T>G (SLC37A4)
ENST00000638360.1:n.1239T>G (SLC37A4)
ENST00000638925.1:n.1372T>G (SLC37A4)
ENST00000650539.1:n.1575T>G (SLC37A4)
ENST00000330775.9:c.1103T>G (SLC37A4) ENSP00000476242.2:p.Ile368Ser
ENST00000357590.9:c.1169T>G (SLC37A4) ENSP00000476176.2:p.Ile390Ser
ENST00000524428.5:n.1339T>G (SLC37A4)
ENST00000525039.5:n.1593T>G (SLC37A4)
ENST00000525102.5:n.1861T>G (SLC37A4)
ENST00000525372.5:n.1201T>G (SLC37A4)
ENST00000526275.5:n.1885T>G (SLC37A4)
ENST00000527992.5:n.1331T>G (SLC37A4)
ENST00000529510.5:n.791T>G (SLC37A4)
ENST00000530407.5:n.1253T>G (SLC37A4)
ENST00000532085.1:n.5121T>G (SLC37A4)
ENST00000533058.5:c.*162A>C (TRAPPC4) ENSP00000432920.1:n.*162A>C
ENST00000538950.5:c.884T>G (SLC37A4) ENSP00000475991.2:p.Ile295Ser
ENST00000545985.5:c.1103T>G (SLC37A4) ENSP00000475241.2:p.Ile368Ser
NM_001164277.1:c.1103T>G , LRG_187t1:c.1103T>G (SLC37A4) NP_001157749.1:p.Ile368Ser
NM_001164278.1:c.1169T>G (SLC37A4) NP_001157750.1:p.Ile390Ser
NM_001164279.1:c.884T>G (SLC37A4) NP_001157751.1:p.Ile295Ser
NM_001164280.1:c.1103T>G (SLC37A4) NP_001157752.1:p.Ile368Ser
NM_001467.5:c.1103T>G (SLC37A4) NP_001458.1:p.Ile368Ser
NM_001164278.2:c.1169T>G (SLC37A4) NP_001157750.1:p.Ile390Ser
NM_001164279.2:c.884T>G (SLC37A4) NP_001157751.1:p.Ile295Ser
NM_001164280.2:c.1103T>G (SLC37A4) NP_001157752.1:p.Ile368Ser
NM_001467.6:c.1103T>G (SLC37A4) NP_001458.1:p.Ile368Ser
NM_001164277.2:c.1103T>G (SLC37A4) MANE Select NP_001157749.1:p.Ile368Ser