Canonical Allele Identifier: CA2003748390

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025199A= , CM000673.2:g.119025199A=	GRCh38
NC_000011.9:g.118895909A= , CM000673.1:g.118895909A=	GRCh37
NC_000011.8:g.118401119A=	NCBI36
NG_013331.1:g.10707T= , LRG_187:g.10707T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1325T= (SLC37A4)
ENST00000697845.1:n.2314T= (SLC37A4)
ENST00000697846.1:n.1687T= (SLC37A4)
ENST00000697847.1:n.1398T= (SLC37A4)
ENST00000697849.1:n.3791T= (SLC37A4)
ENST00000697850.1:n.1982T= (SLC37A4)
ENST00000697851.1:n.2953T= (SLC37A4)
ENST00000638186.1:n.1419T= (SLC37A4)
ENST00000638360.1:n.1251T= (SLC37A4)
ENST00000638925.1:n.1384T= (SLC37A4)
ENST00000650539.1:n.1587T= (SLC37A4)
ENST00000330775.9:c.1115T= (SLC37A4)	ENSP00000476242.2:p.Met372=
ENST00000357590.9:c.1181T= (SLC37A4)	ENSP00000476176.2:p.Met394=
ENST00000524428.5:n.1351T= (SLC37A4)
ENST00000525039.5:n.1605T= (SLC37A4)
ENST00000525102.5:n.1873T= (SLC37A4)
ENST00000525372.5:n.1213T= (SLC37A4)
ENST00000526275.5:n.1897T= (SLC37A4)
ENST00000527992.5:n.1343T= (SLC37A4)
ENST00000529510.5:n.803T= (SLC37A4)
ENST00000530407.5:n.1265T= (SLC37A4)
ENST00000532085.1:n.5133T= (SLC37A4)
ENST00000533058.5:c.*150A= (TRAPPC4)	ENSP00000432920.1:n.*150A=
ENST00000538950.5:c.896T= (SLC37A4)	ENSP00000475991.2:p.Met299=
ENST00000545985.5:c.1115T= (SLC37A4)	ENSP00000475241.2:p.Met372=
NM_001164277.1:c.1115T= , LRG_187t1:c.1115T= (SLC37A4)	NP_001157749.1:p.Met372=
NM_001164278.1:c.1181T= (SLC37A4)	NP_001157750.1:p.Met394=
NM_001164279.1:c.896T= (SLC37A4)	NP_001157751.1:p.Met299=
NM_001164280.1:c.1115T= (SLC37A4)	NP_001157752.1:p.Met372=
NM_001467.5:c.1115T= (SLC37A4)	NP_001458.1:p.Met372=
NM_001164278.2:c.1181T= (SLC37A4)	NP_001157750.1:p.Met394=
NM_001164279.2:c.896T= (SLC37A4)	NP_001157751.1:p.Met299=
NM_001164280.2:c.1115T= (SLC37A4)	NP_001157752.1:p.Met372=
NM_001467.6:c.1115T= (SLC37A4)	NP_001458.1:p.Met372=
NM_001164277.2:c.1115T= (SLC37A4) MANE Select	NP_001157749.1:p.Met372=