Canonical Allele Identifier: CA2003748386

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025193T= , CM000673.2:g.119025193T=	GRCh38
NC_000011.9:g.118895903T= , CM000673.1:g.118895903T=	GRCh37
NC_000011.8:g.118401113T=	NCBI36
NG_013331.1:g.10713A= , LRG_187:g.10713A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1331A= (SLC37A4)
ENST00000697845.1:n.2320A= (SLC37A4)
ENST00000697846.1:n.1693A= (SLC37A4)
ENST00000697847.1:n.1404A= (SLC37A4)
ENST00000697849.1:n.3797A= (SLC37A4)
ENST00000697850.1:n.1988A= (SLC37A4)
ENST00000697851.1:n.2959A= (SLC37A4)
ENST00000638186.1:n.1425A= (SLC37A4)
ENST00000638360.1:n.1257A= (SLC37A4)
ENST00000638925.1:n.1390A= (SLC37A4)
ENST00000650539.1:n.1593A= (SLC37A4)
ENST00000330775.9:c.1121A= (SLC37A4)	ENSP00000476242.2:p.Asn374=
ENST00000357590.9:c.1187A= (SLC37A4)	ENSP00000476176.2:p.Asn396=
ENST00000524428.5:n.1357A= (SLC37A4)
ENST00000525039.5:n.1611A= (SLC37A4)
ENST00000525102.5:n.1879A= (SLC37A4)
ENST00000525372.5:n.1219A= (SLC37A4)
ENST00000526275.5:n.1903A= (SLC37A4)
ENST00000527992.5:n.1349A= (SLC37A4)
ENST00000529510.5:n.809A= (SLC37A4)
ENST00000530407.5:n.1271A= (SLC37A4)
ENST00000532085.1:n.5139A= (SLC37A4)
ENST00000533058.5:c.*144T= (TRAPPC4)	ENSP00000432920.1:n.*144T=
ENST00000538950.5:c.902A= (SLC37A4)	ENSP00000475991.2:p.Asn301=
ENST00000545985.5:c.1121A= (SLC37A4)	ENSP00000475241.2:p.Asn374=
NM_001164277.1:c.1121A= , LRG_187t1:c.1121A= (SLC37A4)	NP_001157749.1:p.Asn374=
NM_001164278.1:c.1187A= (SLC37A4)	NP_001157750.1:p.Asn396=
NM_001164279.1:c.902A= (SLC37A4)	NP_001157751.1:p.Asn301=
NM_001164280.1:c.1121A= (SLC37A4)	NP_001157752.1:p.Asn374=
NM_001467.5:c.1121A= (SLC37A4)	NP_001458.1:p.Asn374=
NM_001164278.2:c.1187A= (SLC37A4)	NP_001157750.1:p.Asn396=
NM_001164279.2:c.902A= (SLC37A4)	NP_001157751.1:p.Asn301=
NM_001164280.2:c.1121A= (SLC37A4)	NP_001157752.1:p.Asn374=
NM_001467.6:c.1121A= (SLC37A4)	NP_001458.1:p.Asn374=
NM_001164277.2:c.1121A= (SLC37A4) MANE Select	NP_001157749.1:p.Asn374=