Canonical Allele Identifier: CA382894810

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895774A>T (hg19) ; chr11:g.119025064A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025064A>T , CM000673.2:g.119025064A>T	GRCh38
NC_000011.9:g.118895774A>T , CM000673.1:g.118895774A>T	GRCh37
NC_000011.8:g.118400984A>T	NCBI36
NG_013331.1:g.10842T>A , LRG_187:g.10842T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1346T>A (SLC37A4)
ENST00000697845.1:n.2335T>A (SLC37A4)
ENST00000697846.1:n.1708T>A (SLC37A4)
ENST00000697847.1:n.1419T>A (SLC37A4)
ENST00000697849.1:n.3812T>A (SLC37A4)
ENST00000697850.1:n.2003T>A (SLC37A4)
ENST00000697851.1:n.2974T>A (SLC37A4)
ENST00000638186.1:n.1440T>A (SLC37A4)
ENST00000638360.1:n.1272T>A (SLC37A4)
ENST00000638925.1:n.1405T>A (SLC37A4)
ENST00000650539.1:n.1608T>A (SLC37A4)
ENST00000330775.9:c.1136T>A (SLC37A4)	ENSP00000476242.2:p.Leu379Gln
ENST00000357590.9:c.1202T>A (SLC37A4)	ENSP00000476176.2:p.Leu401Gln
ENST00000524428.5:n.1372T>A (SLC37A4)
ENST00000525039.5:n.1626T>A (SLC37A4)
ENST00000525102.5:n.1894T>A (SLC37A4)
ENST00000525372.5:n.1234T>A (SLC37A4)
ENST00000526275.5:n.1918T>A (SLC37A4)
ENST00000527992.5:n.1364T>A (SLC37A4)
ENST00000530407.5:n.1286T>A (SLC37A4)
ENST00000532085.1:n.5154T>A (SLC37A4)
ENST00000533058.5:c.*15A>T (TRAPPC4)	ENSP00000432920.1:n.*15A>T
ENST00000538950.5:c.917T>A (SLC37A4)	ENSP00000475991.2:p.Leu306Gln
ENST00000545985.5:c.1136T>A (SLC37A4)	ENSP00000475241.2:p.Leu379Gln
NM_001164277.1:c.1136T>A , LRG_187t1:c.1136T>A (SLC37A4)	NP_001157749.1:p.Leu379Gln
NM_001164278.1:c.1202T>A (SLC37A4)	NP_001157750.1:p.Leu401Gln
NM_001164279.1:c.917T>A (SLC37A4)	NP_001157751.1:p.Leu306Gln
NM_001164280.1:c.1136T>A (SLC37A4)	NP_001157752.1:p.Leu379Gln
NM_001467.5:c.1136T>A (SLC37A4)	NP_001458.1:p.Leu379Gln
NM_001164278.2:c.1202T>A (SLC37A4)	NP_001157750.1:p.Leu401Gln
NM_001164279.2:c.917T>A (SLC37A4)	NP_001157751.1:p.Leu306Gln
NM_001164280.2:c.1136T>A (SLC37A4)	NP_001157752.1:p.Leu379Gln
NM_001467.6:c.1136T>A (SLC37A4)	NP_001458.1:p.Leu379Gln
NM_001164277.2:c.1136T>A (SLC37A4) MANE Select	NP_001157749.1:p.Leu379Gln