Canonical Allele Identifier: CA2003748418

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025251C= , CM000673.2:g.119025251C=	GRCh38
NC_000011.9:g.118895961C= , CM000673.1:g.118895961C=	GRCh37
NC_000011.8:g.118401171C=	NCBI36
NG_013331.1:g.10655G= , LRG_187:g.10655G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001164277.2:c.1063G= (SLC37A4) MANE Select	NP_001157749.1:p.Glu355=
NM_001164277.1:c.1063G= , LRG_187t1:c.1063G= (SLC37A4)	NP_001157749.1:p.Glu355=
NM_001164278.1:c.1129G= (SLC37A4)	NP_001157750.1:p.Glu377=
NM_001164278.2:c.1129G= (SLC37A4)	NP_001157750.1:p.Glu377=
NM_001164279.1:c.844G= (SLC37A4)	NP_001157751.1:p.Glu282=
NM_001164279.2:c.844G= (SLC37A4)	NP_001157751.1:p.Glu282=
NM_001164280.1:c.1063G= (SLC37A4)	NP_001157752.1:p.Glu355=
NM_001164280.2:c.1063G= (SLC37A4)	NP_001157752.1:p.Glu355=
NM_001467.5:c.1063G= (SLC37A4)	NP_001458.1:p.Glu355=
NM_001467.6:c.1063G= (SLC37A4)	NP_001458.1:p.Glu355=
ENST00000330775.9:c.1063G= (SLC37A4)	ENSP00000476242.2:p.Glu355=
ENST00000357590.9:c.1129G= (SLC37A4)	ENSP00000476176.2:p.Glu377=
ENST00000524428.5:n.1299G= (SLC37A4)
ENST00000525039.5:n.1553G= (SLC37A4)
ENST00000525102.5:n.1821G= (SLC37A4)
ENST00000525372.5:n.1161G= (SLC37A4)
ENST00000526275.5:n.1845G= (SLC37A4)
ENST00000527992.5:n.1291G= (SLC37A4)
ENST00000529510.5:n.751G= (SLC37A4)
ENST00000529510.6:n.1273G= (SLC37A4)
ENST00000530407.5:n.1213G= (SLC37A4)
ENST00000532085.1:n.5081G= (SLC37A4)
ENST00000533058.5:c.*202C= (TRAPPC4)	ENSP00000432920.1:n.*202C=
ENST00000538950.5:c.844G= (SLC37A4)	ENSP00000475991.2:p.Glu282=
ENST00000545985.5:c.1063G= (SLC37A4)	ENSP00000475241.2:p.Glu355=
ENST00000638186.1:n.1367G= (SLC37A4)
ENST00000638360.1:n.1199G= (SLC37A4)
ENST00000638925.1:n.1332G= (SLC37A4)
ENST00000650539.1:n.1535G= (SLC37A4)
ENST00000697845.1:n.2262G= (SLC37A4)
ENST00000697846.1:n.1635G= (SLC37A4)
ENST00000697847.1:n.1346G= (SLC37A4)
ENST00000697849.1:n.3739G= (SLC37A4)
ENST00000697850.1:n.1930G= (SLC37A4)
ENST00000697851.1:n.2901G= (SLC37A4)