Canonical Allele Identifier: CA2003748425

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025267A= , CM000673.2:g.119025267A=	GRCh38
NC_000011.9:g.118895977A= , CM000673.1:g.118895977A=	GRCh37
NC_000011.8:g.118401187A=	NCBI36
NG_013331.1:g.10639T= , LRG_187:g.10639T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1257T= (SLC37A4)
ENST00000697845.1:n.2246T= (SLC37A4)
ENST00000697846.1:n.1619T= (SLC37A4)
ENST00000697847.1:n.1330T= (SLC37A4)
ENST00000697849.1:n.3723T= (SLC37A4)
ENST00000697850.1:n.1914T= (SLC37A4)
ENST00000697851.1:n.2885T= (SLC37A4)
ENST00000638186.1:n.1351T= (SLC37A4)
ENST00000638360.1:n.1183T= (SLC37A4)
ENST00000638925.1:n.1316T= (SLC37A4)
ENST00000650539.1:n.1519T= (SLC37A4)
ENST00000330775.9:c.1047T= (SLC37A4)	ENSP00000476242.2:p.Phe349=
ENST00000357590.9:c.1113T= (SLC37A4)	ENSP00000476176.2:p.Phe371=
ENST00000524428.5:n.1283T= (SLC37A4)
ENST00000525039.5:n.1537T= (SLC37A4)
ENST00000525102.5:n.1805T= (SLC37A4)
ENST00000525372.5:n.1145T= (SLC37A4)
ENST00000526275.5:n.1829T= (SLC37A4)
ENST00000527992.5:n.1275T= (SLC37A4)
ENST00000529510.5:n.735T= (SLC37A4)
ENST00000530407.5:n.1197T= (SLC37A4)
ENST00000532085.1:n.5065T= (SLC37A4)
ENST00000533058.5:c.*218A= (TRAPPC4)	ENSP00000432920.1:n.*218A=
ENST00000538950.5:c.828T= (SLC37A4)	ENSP00000475991.2:p.Phe276=
ENST00000545985.5:c.1047T= (SLC37A4)	ENSP00000475241.2:p.Phe349=
NM_001164277.1:c.1047T= , LRG_187t1:c.1047T= (SLC37A4)	NP_001157749.1:p.Phe349=
NM_001164278.1:c.1113T= (SLC37A4)	NP_001157750.1:p.Phe371=
NM_001164279.1:c.828T= (SLC37A4)	NP_001157751.1:p.Phe276=
NM_001164280.1:c.1047T= (SLC37A4)	NP_001157752.1:p.Phe349=
NM_001467.5:c.1047T= (SLC37A4)	NP_001458.1:p.Phe349=
NM_001164278.2:c.1113T= (SLC37A4)	NP_001157750.1:p.Phe371=
NM_001164279.2:c.828T= (SLC37A4)	NP_001157751.1:p.Phe276=
NM_001164280.2:c.1047T= (SLC37A4)	NP_001157752.1:p.Phe349=
NM_001467.6:c.1047T= (SLC37A4)	NP_001458.1:p.Phe349=
NM_001164277.2:c.1047T= (SLC37A4) MANE Select	NP_001157749.1:p.Phe349=