Canonical Allele Identifier: CA2003748135
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1943495276

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024730A>G , CM000673.2:g.119024730A>G GRCh38
NC_000011.9:g.118895440A>G , CM000673.1:g.118895440A>G GRCh37
NC_000011.8:g.118400650A>G NCBI36
NG_013331.1:g.11176T>C , LRG_187:g.11176T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1680T>C (SLC37A4)
ENST00000697845.1:n.2669T>C (SLC37A4)
ENST00000697846.1:n.2042T>C (SLC37A4)
ENST00000697847.1:n.1753T>C (SLC37A4)
ENST00000697849.1:n.4146T>C (SLC37A4)
ENST00000697850.1:n.2337T>C (SLC37A4)
ENST00000697851.1:n.3308T>C (SLC37A4)
ENST00000638186.1:n.1774T>C (SLC37A4)
ENST00000638360.1:n.1606T>C (SLC37A4)
ENST00000638925.1:n.1739T>C (SLC37A4)
ENST00000650539.1:n.1942T>C (SLC37A4)
ENST00000330775.9:c.*180T>C (SLC37A4) ENSP00000476242.2:n.*180T>C
ENST00000357590.9:c.*180T>C (SLC37A4) ENSP00000476176.2:n.*180T>C
ENST00000525102.5:n.2228T>C (SLC37A4)
ENST00000526275.5:n.2252T>C (SLC37A4)
ENST00000527992.5:n.1698T>C (SLC37A4)
ENST00000532085.1:n.5488T>C (SLC37A4)
ENST00000533058.5:c.582-127A>G (TRAPPC4) ENSP00000432920.1:n.582-127A>G
ENST00000538950.5:c.*180T>C (SLC37A4) ENSP00000475991.2:n.*180T>C
ENST00000545985.5:c.*180T>C (SLC37A4) ENSP00000475241.2:n.*180T>C
NM_001164277.1:c.*180T>C , LRG_187t1:c.*180T>C (SLC37A4) NP_001157749.1:n.*180T>C
NM_001164278.1:c.*180T>C (SLC37A4) NP_001157750.1:n.*180T>C
NM_001164279.1:c.*180T>C (SLC37A4) NP_001157751.1:n.*180T>C
NM_001164280.1:c.*180T>C (SLC37A4) NP_001157752.1:n.*180T>C
NM_001467.5:c.*180T>C (SLC37A4) NP_001458.1:n.*180T>C
NM_001164278.2:c.*180T>C (SLC37A4) NP_001157750.1:n.*180T>C
NM_001164279.2:c.*180T>C (SLC37A4) NP_001157751.1:n.*180T>C
NM_001164280.2:c.*180T>C (SLC37A4) NP_001157752.1:n.*180T>C
NM_001467.6:c.*180T>C (SLC37A4) NP_001458.1:n.*180T>C
NM_001164277.2:c.*180T>C (SLC37A4) MANE Select NP_001157749.1:n.*180T>C