Canonical Allele Identifier: CA2003748074

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024633G= , CM000673.2:g.119024633G=	GRCh38
NC_000011.9:g.118895343G= , CM000673.1:g.118895343G=	GRCh37
NC_000011.8:g.118400553G=	NCBI36
NG_013331.1:g.11273C= , LRG_187:g.11273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1777C= (SLC37A4)
ENST00000697845.1:n.2766C= (SLC37A4)
ENST00000697846.1:n.2139C= (SLC37A4)
ENST00000697847.1:n.1850C= (SLC37A4)
ENST00000697849.1:n.4243C= (SLC37A4)
ENST00000697850.1:n.2434C= (SLC37A4)
ENST00000697851.1:n.3405C= (SLC37A4)
ENST00000638186.1:n.1871C= (SLC37A4)
ENST00000638360.1:n.1703C= (SLC37A4)
ENST00000638925.1:n.1836C= (SLC37A4)
ENST00000650539.1:n.2039C= (SLC37A4)
ENST00000330775.9:c.*277C= (SLC37A4)	ENSP00000476242.2:n.*277C=
ENST00000357590.9:c.*277C= (SLC37A4)	ENSP00000476176.2:n.*277C=
ENST00000525102.5:n.2325C= (SLC37A4)
ENST00000526275.5:n.2349C= (SLC37A4)
ENST00000527992.5:n.1795C= (SLC37A4)
ENST00000532085.1:n.5585C= (SLC37A4)
ENST00000533058.5:c.582-224G= (TRAPPC4)	ENSP00000432920.1:n.582-224G=
ENST00000538950.5:c.*277C= (SLC37A4)	ENSP00000475991.2:n.*277C=
ENST00000545985.5:c.*277C= (SLC37A4)	ENSP00000475241.2:n.*277C=
NM_001164277.1:c.*277C= , LRG_187t1:c.*277C= (SLC37A4)	NP_001157749.1:n.*277C=
NM_001164278.1:c.*277C= (SLC37A4)	NP_001157750.1:n.*277C=
NM_001164279.1:c.*277C= (SLC37A4)	NP_001157751.1:n.*277C=
NM_001164280.1:c.*277C= (SLC37A4)	NP_001157752.1:n.*277C=
NM_001467.5:c.*277C= (SLC37A4)	NP_001458.1:n.*277C=
NM_001164278.2:c.*277C= (SLC37A4)	NP_001157750.1:n.*277C=
NM_001164279.2:c.*277C= (SLC37A4)	NP_001157751.1:n.*277C=
NM_001164280.2:c.*277C= (SLC37A4)	NP_001157752.1:n.*277C=
NM_001467.6:c.*277C= (SLC37A4)	NP_001458.1:n.*277C=
NM_001164277.2:c.*277C= (SLC37A4) MANE Select	NP_001157749.1:n.*277C=