Canonical Allele Identifier: CA2003748297

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025027G= , CM000673.2:g.119025027G=	GRCh38
NC_000011.9:g.118895737G= , CM000673.1:g.118895737G=	GRCh37
NC_000011.8:g.118400947G=	NCBI36
NG_013331.1:g.10879C= , LRG_187:g.10879C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1383C= (SLC37A4)
ENST00000697845.1:n.2372C= (SLC37A4)
ENST00000697846.1:n.1745C= (SLC37A4)
ENST00000697847.1:n.1456C= (SLC37A4)
ENST00000697849.1:n.3849C= (SLC37A4)
ENST00000697850.1:n.2040C= (SLC37A4)
ENST00000697851.1:n.3011C= (SLC37A4)
ENST00000638186.1:n.1477C= (SLC37A4)
ENST00000638360.1:n.1309C= (SLC37A4)
ENST00000638925.1:n.1442C= (SLC37A4)
ENST00000650539.1:n.1645C= (SLC37A4)
ENST00000330775.9:c.1173C= (SLC37A4)	ENSP00000476242.2:p.Tyr391=
ENST00000357590.9:c.1239C= (SLC37A4)	ENSP00000476176.2:p.Tyr413=
ENST00000524428.5:n.1409C= (SLC37A4)
ENST00000525039.5:n.1663C= (SLC37A4)
ENST00000525102.5:n.1931C= (SLC37A4)
ENST00000525372.5:n.1271C= (SLC37A4)
ENST00000526275.5:n.1955C= (SLC37A4)
ENST00000527992.5:n.1401C= (SLC37A4)
ENST00000530407.5:n.1323C= (SLC37A4)
ENST00000532085.1:n.5191C= (SLC37A4)
ENST00000533058.5:c.752G= (TRAPPC4)	ENSP00000432920.1:p.Cys251=
ENST00000538950.5:c.954C= (SLC37A4)	ENSP00000475991.2:p.Tyr318=
ENST00000545985.5:c.1173C= (SLC37A4)	ENSP00000475241.2:p.Tyr391=
NM_001164277.1:c.1173C= , LRG_187t1:c.1173C= (SLC37A4)	NP_001157749.1:p.Tyr391=
NM_001164278.1:c.1239C= (SLC37A4)	NP_001157750.1:p.Tyr413=
NM_001164279.1:c.954C= (SLC37A4)	NP_001157751.1:p.Tyr318=
NM_001164280.1:c.1173C= (SLC37A4)	NP_001157752.1:p.Tyr391=
NM_001467.5:c.1173C= (SLC37A4)	NP_001458.1:p.Tyr391=
NM_001164278.2:c.1239C= (SLC37A4)	NP_001157750.1:p.Tyr413=
NM_001164279.2:c.954C= (SLC37A4)	NP_001157751.1:p.Tyr318=
NM_001164280.2:c.1173C= (SLC37A4)	NP_001157752.1:p.Tyr391=
NM_001467.6:c.1173C= (SLC37A4)	NP_001458.1:p.Tyr391=
NM_001164277.2:c.1173C= (SLC37A4) MANE Select	NP_001157749.1:p.Tyr391=