Canonical Allele Identifier: CA2616339306
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024597del , CM000673.2:g.119024597del GRCh38
NC_000011.9:g.118895307del , CM000673.1:g.118895307del GRCh37
NC_000011.8:g.118400517del NCBI36
NG_013331.1:g.11309del , LRG_187:g.11309del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1813del (SLC37A4)
ENST00000697845.1:n.2802del (SLC37A4)
ENST00000697846.1:n.2175del (SLC37A4)
ENST00000697847.1:n.1886del (SLC37A4)
ENST00000697849.1:n.4279del (SLC37A4)
ENST00000697850.1:n.2470del (SLC37A4)
ENST00000697851.1:n.3441del (SLC37A4)
ENST00000638186.1:n.1907del (SLC37A4)
ENST00000638360.1:n.1739del (SLC37A4)
ENST00000638925.1:n.1872del (SLC37A4)
ENST00000650539.1:n.2075del (SLC37A4)
ENST00000330775.9:c.*313del (SLC37A4) ENSP00000476242.2:n.*313del
ENST00000357590.9:c.*313del (SLC37A4) ENSP00000476176.2:n.*313del
ENST00000525102.5:n.2361del (SLC37A4)
ENST00000526275.5:n.2385del (SLC37A4)
ENST00000527992.5:n.1831del (SLC37A4)
ENST00000532085.1:n.5621del (SLC37A4)
ENST00000533058.5:c.582-260del (TRAPPC4) ENSP00000432920.1:n.582-260del
ENST00000538950.5:c.*313del (SLC37A4) ENSP00000475991.2:n.*313del
ENST00000545985.5:c.*313del (SLC37A4) ENSP00000475241.2:n.*313del
NM_001164277.1:c.*313del , LRG_187t1:c.*313del (SLC37A4) NP_001157749.1:n.*313del
NM_001164278.1:c.*313del (SLC37A4) NP_001157750.1:n.*313del
NM_001164279.1:c.*313del (SLC37A4) NP_001157751.1:n.*313del
NM_001164280.1:c.*313del (SLC37A4) NP_001157752.1:n.*313del
NM_001467.5:c.*313del (SLC37A4) NP_001458.1:n.*313del
NM_001164278.2:c.*313del (SLC37A4) NP_001157750.1:n.*313del
NM_001164279.2:c.*313del (SLC37A4) NP_001157751.1:n.*313del
NM_001164280.2:c.*313del (SLC37A4) NP_001157752.1:n.*313del
NM_001467.6:c.*313del (SLC37A4) NP_001458.1:n.*313del
NM_001164277.2:c.*313del (SLC37A4) MANE Select NP_001157749.1:n.*313del