Canonical Allele Identifier: CA382892782
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1308702608

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024882G>A , CM000673.2:g.119024882G>A GRCh38
NC_000011.9:g.118895592G>A , CM000673.1:g.118895592G>A GRCh37
NC_000011.8:g.118400802G>A NCBI36
NG_013331.1:g.11024C>T , LRG_187:g.11024C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1528C>T (SLC37A4)
ENST00000697845.1:n.2517C>T (SLC37A4)
ENST00000697846.1:n.1890C>T (SLC37A4)
ENST00000697847.1:n.1601C>T (SLC37A4)
ENST00000697849.1:n.3994C>T (SLC37A4)
ENST00000697850.1:n.2185C>T (SLC37A4)
ENST00000697851.1:n.3156C>T (SLC37A4)
ENST00000638186.1:n.1622C>T (SLC37A4)
ENST00000638360.1:n.1454C>T (SLC37A4)
ENST00000638925.1:n.1587C>T (SLC37A4)
ENST00000650539.1:n.1790C>T (SLC37A4)
ENST00000330775.9:c.*28C>T (SLC37A4) ENSP00000476242.2:n.*28C>T
ENST00000357590.9:c.*28C>T (SLC37A4) ENSP00000476176.2:n.*28C>T
ENST00000525102.5:n.2076C>T (SLC37A4)
ENST00000526275.5:n.2100C>T (SLC37A4)
ENST00000527992.5:n.1546C>T (SLC37A4)
ENST00000530407.5:n.1468C>T (SLC37A4)
ENST00000532085.1:n.5336C>T (SLC37A4)
ENST00000533058.5:c.607G>A (TRAPPC4) ENSP00000432920.1:p.Gly203Arg
ENST00000538950.5:c.*28C>T (SLC37A4) ENSP00000475991.2:n.*28C>T
ENST00000545985.5:c.*28C>T (SLC37A4) ENSP00000475241.2:n.*28C>T
NM_001164277.1:c.*28C>T , LRG_187t1:c.*28C>T (SLC37A4) NP_001157749.1:n.*28C>T
NM_001164278.1:c.*28C>T (SLC37A4) NP_001157750.1:n.*28C>T
NM_001164279.1:c.*28C>T (SLC37A4) NP_001157751.1:n.*28C>T
NM_001164280.1:c.*28C>T (SLC37A4) NP_001157752.1:n.*28C>T
NM_001467.5:c.*28C>T (SLC37A4) NP_001458.1:n.*28C>T
NM_001164278.2:c.*28C>T (SLC37A4) NP_001157750.1:n.*28C>T
NM_001164279.2:c.*28C>T (SLC37A4) NP_001157751.1:n.*28C>T
NM_001164280.2:c.*28C>T (SLC37A4) NP_001157752.1:n.*28C>T
NM_001467.6:c.*28C>T (SLC37A4) NP_001458.1:n.*28C>T
NM_001164277.2:c.*28C>T (SLC37A4) MANE Select NP_001157749.1:n.*28C>T