Canonical Allele Identifier: CA2003748414

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025246A= , CM000673.2:g.119025246A=	GRCh38
NC_000011.9:g.118895956A= , CM000673.1:g.118895956A=	GRCh37
NC_000011.8:g.118401166A=	NCBI36
NG_013331.1:g.10660T= , LRG_187:g.10660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1278T= (SLC37A4)
ENST00000697845.1:n.2267T= (SLC37A4)
ENST00000697846.1:n.1640T= (SLC37A4)
ENST00000697847.1:n.1351T= (SLC37A4)
ENST00000697849.1:n.3744T= (SLC37A4)
ENST00000697850.1:n.1935T= (SLC37A4)
ENST00000697851.1:n.2906T= (SLC37A4)
ENST00000638186.1:n.1372T= (SLC37A4)
ENST00000638360.1:n.1204T= (SLC37A4)
ENST00000638925.1:n.1337T= (SLC37A4)
ENST00000650539.1:n.1540T= (SLC37A4)
ENST00000330775.9:c.1068T= (SLC37A4)	ENSP00000476242.2:p.Ser356=
ENST00000357590.9:c.1134T= (SLC37A4)	ENSP00000476176.2:p.Ser378=
ENST00000524428.5:n.1304T= (SLC37A4)
ENST00000525039.5:n.1558T= (SLC37A4)
ENST00000525102.5:n.1826T= (SLC37A4)
ENST00000525372.5:n.1166T= (SLC37A4)
ENST00000526275.5:n.1850T= (SLC37A4)
ENST00000527992.5:n.1296T= (SLC37A4)
ENST00000529510.5:n.756T= (SLC37A4)
ENST00000530407.5:n.1218T= (SLC37A4)
ENST00000532085.1:n.5086T= (SLC37A4)
ENST00000533058.5:c.*197A= (TRAPPC4)	ENSP00000432920.1:n.*197A=
ENST00000538950.5:c.849T= (SLC37A4)	ENSP00000475991.2:p.Ser283=
ENST00000545985.5:c.1068T= (SLC37A4)	ENSP00000475241.2:p.Ser356=
NM_001164277.1:c.1068T= , LRG_187t1:c.1068T= (SLC37A4)	NP_001157749.1:p.Ser356=
NM_001164278.1:c.1134T= (SLC37A4)	NP_001157750.1:p.Ser378=
NM_001164279.1:c.849T= (SLC37A4)	NP_001157751.1:p.Ser283=
NM_001164280.1:c.1068T= (SLC37A4)	NP_001157752.1:p.Ser356=
NM_001467.5:c.1068T= (SLC37A4)	NP_001458.1:p.Ser356=
NM_001164278.2:c.1134T= (SLC37A4)	NP_001157750.1:p.Ser378=
NM_001164279.2:c.849T= (SLC37A4)	NP_001157751.1:p.Ser283=
NM_001164280.2:c.1068T= (SLC37A4)	NP_001157752.1:p.Ser356=
NM_001467.6:c.1068T= (SLC37A4)	NP_001458.1:p.Ser356=
NM_001164277.2:c.1068T= (SLC37A4) MANE Select	NP_001157749.1:p.Ser356=