Canonical Allele Identifier: CA2695215876

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025255_119025267delinsATAGCC , CM000673.2:g.119025255_119025267delinsATAGCC	GRCh38
NC_000011.9:g.118895965_118895977delinsATAGCC , CM000673.1:g.118895965_118895977delinsATAGCC	GRCh37
NC_000011.8:g.118401175_118401187delinsATAGCC	NCBI36
NG_013331.1:g.10639_10651delinsGGCTAT , LRG_187:g.10639_10651delinsGGCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1257_1269delinsGGCTAT (SLC37A4)
ENST00000697845.1:n.2246_2258delinsGGCTAT (SLC37A4)
ENST00000697846.1:n.1619_1631delinsGGCTAT (SLC37A4)
ENST00000697847.1:n.1330_1342delinsGGCTAT (SLC37A4)
ENST00000697849.1:n.3723_3735delinsGGCTAT (SLC37A4)
ENST00000697850.1:n.1914_1926delinsGGCTAT (SLC37A4)
ENST00000697851.1:n.2885_2897delinsGGCTAT (SLC37A4)
ENST00000638186.1:n.1351_1363delinsGGCTAT (SLC37A4)
ENST00000638360.1:n.1183_1195delinsGGCTAT (SLC37A4)
ENST00000638925.1:n.1316_1328delinsGGCTAT (SLC37A4)
ENST00000650539.1:n.1519_1531delinsGGCTAT (SLC37A4)
ENST00000330775.9:c.1047_1059delinsGGCTAT (SLC37A4)	ENSP00000476242.2:p.Phe349LeufsTer?
ENST00000357590.9:c.1113_1125delinsGGCTAT (SLC37A4)	ENSP00000476176.2:p.Phe371LeufsTer?
ENST00000524428.5:n.1283_1295delinsGGCTAT (SLC37A4)
ENST00000525039.5:n.1537_1549delinsGGCTAT (SLC37A4)
ENST00000525102.5:n.1805_1817delinsGGCTAT (SLC37A4)
ENST00000525372.5:n.1145_1157delinsGGCTAT (SLC37A4)
ENST00000526275.5:n.1829_1841delinsGGCTAT (SLC37A4)
ENST00000527992.5:n.1275_1287delinsGGCTAT (SLC37A4)
ENST00000529510.5:n.735_747delinsGGCTAT (SLC37A4)
ENST00000530407.5:n.1197_1209delinsGGCTAT (SLC37A4)
ENST00000532085.1:n.5065_5077delinsGGCTAT (SLC37A4)
ENST00000533058.5:c.*206_*218delinsATAGCC (TRAPPC4)	ENSP00000432920.1:n.*206_*218delinsATAGCC
ENST00000538950.5:c.828_840delinsGGCTAT (SLC37A4)	ENSP00000475991.2:p.Phe276LeufsTer?
ENST00000545985.5:c.1047_1059delinsGGCTAT (SLC37A4)	ENSP00000475241.2:p.Phe349LeufsTer?
NM_001164277.1:c.1047_1059delinsGGCTAT , LRG_187t1:c.1047_1059delinsGGCTAT (SLC37A4)	NP_001157749.1:p.Phe349LeufsTer?
NM_001164278.1:c.1113_1125delinsGGCTAT (SLC37A4)	NP_001157750.1:p.Phe371LeufsTer?
NM_001164279.1:c.828_840delinsGGCTAT (SLC37A4)	NP_001157751.1:p.Phe276LeufsTer?
NM_001164280.1:c.1047_1059delinsGGCTAT (SLC37A4)	NP_001157752.1:p.Phe349LeufsTer?
NM_001467.5:c.1047_1059delinsGGCTAT (SLC37A4)	NP_001458.1:p.Phe349LeufsTer?
NM_001164278.2:c.1113_1125delinsGGCTAT (SLC37A4)	NP_001157750.1:p.Phe371LeufsTer?
NM_001164279.2:c.828_840delinsGGCTAT (SLC37A4)	NP_001157751.1:p.Phe276LeufsTer?
NM_001164280.2:c.1047_1059delinsGGCTAT (SLC37A4)	NP_001157752.1:p.Phe349LeufsTer?
NM_001467.6:c.1047_1059delinsGGCTAT (SLC37A4)	NP_001458.1:p.Phe349LeufsTer?
NM_001164277.2:c.1047_1059delinsGGCTAT (SLC37A4) MANE Select	NP_001157749.1:p.Phe349LeufsTer?