Canonical Allele Identifier: CA2003748155
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1943496335

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024770G>T , CM000673.2:g.119024770G>T GRCh38
NC_000011.9:g.118895480G>T , CM000673.1:g.118895480G>T GRCh37
NC_000011.8:g.118400690G>T NCBI36
NG_013331.1:g.11136C>A , LRG_187:g.11136C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1640C>A (SLC37A4)
ENST00000697845.1:n.2629C>A (SLC37A4)
ENST00000697846.1:n.2002C>A (SLC37A4)
ENST00000697847.1:n.1713C>A (SLC37A4)
ENST00000697849.1:n.4106C>A (SLC37A4)
ENST00000697850.1:n.2297C>A (SLC37A4)
ENST00000697851.1:n.3268C>A (SLC37A4)
ENST00000638186.1:n.1734C>A (SLC37A4)
ENST00000638360.1:n.1566C>A (SLC37A4)
ENST00000638925.1:n.1699C>A (SLC37A4)
ENST00000650539.1:n.1902C>A (SLC37A4)
ENST00000330775.9:c.*140C>A (SLC37A4) ENSP00000476242.2:n.*140C>A
ENST00000357590.9:c.*140C>A (SLC37A4) ENSP00000476176.2:n.*140C>A
ENST00000525102.5:n.2188C>A (SLC37A4)
ENST00000526275.5:n.2212C>A (SLC37A4)
ENST00000527992.5:n.1658C>A (SLC37A4)
ENST00000532085.1:n.5448C>A (SLC37A4)
ENST00000533058.5:c.582-87G>T (TRAPPC4) ENSP00000432920.1:n.582-87G>T
ENST00000538950.5:c.*140C>A (SLC37A4) ENSP00000475991.2:n.*140C>A
ENST00000545985.5:c.*140C>A (SLC37A4) ENSP00000475241.2:n.*140C>A
NM_001164277.1:c.*140C>A , LRG_187t1:c.*140C>A (SLC37A4) NP_001157749.1:n.*140C>A
NM_001164278.1:c.*140C>A (SLC37A4) NP_001157750.1:n.*140C>A
NM_001164279.1:c.*140C>A (SLC37A4) NP_001157751.1:n.*140C>A
NM_001164280.1:c.*140C>A (SLC37A4) NP_001157752.1:n.*140C>A
NM_001467.5:c.*140C>A (SLC37A4) NP_001458.1:n.*140C>A
NM_001164278.2:c.*140C>A (SLC37A4) NP_001157750.1:n.*140C>A
NM_001164279.2:c.*140C>A (SLC37A4) NP_001157751.1:n.*140C>A
NM_001164280.2:c.*140C>A (SLC37A4) NP_001157752.1:n.*140C>A
NM_001467.6:c.*140C>A (SLC37A4) NP_001458.1:n.*140C>A
NM_001164277.2:c.*140C>A (SLC37A4) MANE Select NP_001157749.1:n.*140C>A