Canonical Allele Identifier: CA382894748

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895765A>T (hg19) ; chr11:g.119025055A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025055A>T , CM000673.2:g.119025055A>T	GRCh38
NC_000011.9:g.118895765A>T , CM000673.1:g.118895765A>T	GRCh37
NC_000011.8:g.118400975A>T	NCBI36
NG_013331.1:g.10851T>A , LRG_187:g.10851T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1355T>A (SLC37A4)
ENST00000697845.1:n.2344T>A (SLC37A4)
ENST00000697846.1:n.1717T>A (SLC37A4)
ENST00000697847.1:n.1428T>A (SLC37A4)
ENST00000697849.1:n.3821T>A (SLC37A4)
ENST00000697850.1:n.2012T>A (SLC37A4)
ENST00000697851.1:n.2983T>A (SLC37A4)
ENST00000638186.1:n.1449T>A (SLC37A4)
ENST00000638360.1:n.1281T>A (SLC37A4)
ENST00000638925.1:n.1414T>A (SLC37A4)
ENST00000650539.1:n.1617T>A (SLC37A4)
ENST00000330775.9:c.1145T>A (SLC37A4)	ENSP00000476242.2:p.Leu382Gln
ENST00000357590.9:c.1211T>A (SLC37A4)	ENSP00000476176.2:p.Leu404Gln
ENST00000524428.5:n.1381T>A (SLC37A4)
ENST00000525039.5:n.1635T>A (SLC37A4)
ENST00000525102.5:n.1903T>A (SLC37A4)
ENST00000525372.5:n.1243T>A (SLC37A4)
ENST00000526275.5:n.1927T>A (SLC37A4)
ENST00000527992.5:n.1373T>A (SLC37A4)
ENST00000530407.5:n.1295T>A (SLC37A4)
ENST00000532085.1:n.5163T>A (SLC37A4)
ENST00000533058.5:c.*6A>T (TRAPPC4)	ENSP00000432920.1:n.*6A>T
ENST00000538950.5:c.926T>A (SLC37A4)	ENSP00000475991.2:p.Leu309Gln
ENST00000545985.5:c.1145T>A (SLC37A4)	ENSP00000475241.2:p.Leu382Gln
NM_001164277.1:c.1145T>A , LRG_187t1:c.1145T>A (SLC37A4)	NP_001157749.1:p.Leu382Gln
NM_001164278.1:c.1211T>A (SLC37A4)	NP_001157750.1:p.Leu404Gln
NM_001164279.1:c.926T>A (SLC37A4)	NP_001157751.1:p.Leu309Gln
NM_001164280.1:c.1145T>A (SLC37A4)	NP_001157752.1:p.Leu382Gln
NM_001467.5:c.1145T>A (SLC37A4)	NP_001458.1:p.Leu382Gln
NM_001164278.2:c.1211T>A (SLC37A4)	NP_001157750.1:p.Leu404Gln
NM_001164279.2:c.926T>A (SLC37A4)	NP_001157751.1:p.Leu309Gln
NM_001164280.2:c.1145T>A (SLC37A4)	NP_001157752.1:p.Leu382Gln
NM_001467.6:c.1145T>A (SLC37A4)	NP_001458.1:p.Leu382Gln
NM_001164277.2:c.1145T>A (SLC37A4) MANE Select	NP_001157749.1:p.Leu382Gln