Canonical Allele Identifier: CA382894789

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895771G>T (hg19) ; chr11:g.119025061G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025061G>T , CM000673.2:g.119025061G>T	GRCh38
NC_000011.9:g.118895771G>T , CM000673.1:g.118895771G>T	GRCh37
NC_000011.8:g.118400981G>T	NCBI36
NG_013331.1:g.10845C>A , LRG_187:g.10845C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1349C>A (SLC37A4)
ENST00000697845.1:n.2338C>A (SLC37A4)
ENST00000697846.1:n.1711C>A (SLC37A4)
ENST00000697847.1:n.1422C>A (SLC37A4)
ENST00000697849.1:n.3815C>A (SLC37A4)
ENST00000697850.1:n.2006C>A (SLC37A4)
ENST00000697851.1:n.2977C>A (SLC37A4)
ENST00000638186.1:n.1443C>A (SLC37A4)
ENST00000638360.1:n.1275C>A (SLC37A4)
ENST00000638925.1:n.1408C>A (SLC37A4)
ENST00000650539.1:n.1611C>A (SLC37A4)
ENST00000330775.9:c.1139C>A (SLC37A4)	ENSP00000476242.2:p.Ala380Asp
ENST00000357590.9:c.1205C>A (SLC37A4)	ENSP00000476176.2:p.Ala402Asp
ENST00000524428.5:n.1375C>A (SLC37A4)
ENST00000525039.5:n.1629C>A (SLC37A4)
ENST00000525102.5:n.1897C>A (SLC37A4)
ENST00000525372.5:n.1237C>A (SLC37A4)
ENST00000526275.5:n.1921C>A (SLC37A4)
ENST00000527992.5:n.1367C>A (SLC37A4)
ENST00000530407.5:n.1289C>A (SLC37A4)
ENST00000532085.1:n.5157C>A (SLC37A4)
ENST00000533058.5:c.*12G>T (TRAPPC4)	ENSP00000432920.1:n.*12G>T
ENST00000538950.5:c.920C>A (SLC37A4)	ENSP00000475991.2:p.Ala307Asp
ENST00000545985.5:c.1139C>A (SLC37A4)	ENSP00000475241.2:p.Ala380Asp
NM_001164277.1:c.1139C>A , LRG_187t1:c.1139C>A (SLC37A4)	NP_001157749.1:p.Ala380Asp
NM_001164278.1:c.1205C>A (SLC37A4)	NP_001157750.1:p.Ala402Asp
NM_001164279.1:c.920C>A (SLC37A4)	NP_001157751.1:p.Ala307Asp
NM_001164280.1:c.1139C>A (SLC37A4)	NP_001157752.1:p.Ala380Asp
NM_001467.5:c.1139C>A (SLC37A4)	NP_001458.1:p.Ala380Asp
NM_001164278.2:c.1205C>A (SLC37A4)	NP_001157750.1:p.Ala402Asp
NM_001164279.2:c.920C>A (SLC37A4)	NP_001157751.1:p.Ala307Asp
NM_001164280.2:c.1139C>A (SLC37A4)	NP_001157752.1:p.Ala380Asp
NM_001467.6:c.1139C>A (SLC37A4)	NP_001458.1:p.Ala380Asp
NM_001164277.2:c.1139C>A (SLC37A4) MANE Select	NP_001157749.1:p.Ala380Asp