Canonical Allele Identifier: CA2003748457
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025317C= , CM000673.2:g.119025317C= GRCh38
NC_000011.9:g.118896027C= , CM000673.1:g.118896027C= GRCh37
NC_000011.8:g.118401237C= NCBI36
NG_013331.1:g.10589G= , LRG_187:g.10589G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1207G= (SLC37A4)
ENST00000697845.1:n.2196G= (SLC37A4)
ENST00000697846.1:n.1569G= (SLC37A4)
ENST00000697847.1:n.1280G= (SLC37A4)
ENST00000697849.1:n.3673G= (SLC37A4)
ENST00000697850.1:n.1864G= (SLC37A4)
ENST00000697851.1:n.2835G= (SLC37A4)
ENST00000638186.1:n.1301G= (SLC37A4)
ENST00000638360.1:n.1133G= (SLC37A4)
ENST00000638925.1:n.1266G= (SLC37A4)
ENST00000650539.1:n.1469G= (SLC37A4)
ENST00000330775.9:c.997G= (SLC37A4) ENSP00000476242.2:p.Val333=
ENST00000357590.9:c.1063G= (SLC37A4) ENSP00000476176.2:p.Val355=
ENST00000524428.5:n.1233G= (SLC37A4)
ENST00000525039.5:n.1487G= (SLC37A4)
ENST00000525102.5:n.1755G= (SLC37A4)
ENST00000525372.5:n.1095G= (SLC37A4)
ENST00000526275.5:n.1779G= (SLC37A4)
ENST00000527992.5:n.1225G= (SLC37A4)
ENST00000529510.5:n.685G= (SLC37A4)
ENST00000530407.5:n.1147G= (SLC37A4)
ENST00000532085.1:n.5015G= (SLC37A4)
ENST00000533058.5:c.*268C= (TRAPPC4) ENSP00000432920.1:n.*268C=
ENST00000538950.5:c.778G= (SLC37A4) ENSP00000475991.2:p.Val260=
ENST00000545985.5:c.997G= (SLC37A4) ENSP00000475241.2:p.Val333=
NM_001164277.1:c.997G= , LRG_187t1:c.997G= (SLC37A4) NP_001157749.1:p.Val333=
NM_001164278.1:c.1063G= (SLC37A4) NP_001157750.1:p.Val355=
NM_001164279.1:c.778G= (SLC37A4) NP_001157751.1:p.Val260=
NM_001164280.1:c.997G= (SLC37A4) NP_001157752.1:p.Val333=
NM_001467.5:c.997G= (SLC37A4) NP_001458.1:p.Val333=
NM_001164278.2:c.1063G= (SLC37A4) NP_001157750.1:p.Val355=
NM_001164279.2:c.778G= (SLC37A4) NP_001157751.1:p.Val260=
NM_001164280.2:c.997G= (SLC37A4) NP_001157752.1:p.Val333=
NM_001467.6:c.997G= (SLC37A4) NP_001458.1:p.Val333=
NM_001164277.2:c.997G= (SLC37A4) MANE Select NP_001157749.1:p.Val333=