Canonical Allele Identifier: CA382895276

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895918A>G (hg19) ; chr11:g.119025208A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025208A>G , CM000673.2:g.119025208A>G	GRCh38
NC_000011.9:g.118895918A>G , CM000673.1:g.118895918A>G	GRCh37
NC_000011.8:g.118401128A>G	NCBI36
NG_013331.1:g.10698T>C , LRG_187:g.10698T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1316T>C (SLC37A4)
ENST00000697845.1:n.2305T>C (SLC37A4)
ENST00000697846.1:n.1678T>C (SLC37A4)
ENST00000697847.1:n.1389T>C (SLC37A4)
ENST00000697849.1:n.3782T>C (SLC37A4)
ENST00000697850.1:n.1973T>C (SLC37A4)
ENST00000697851.1:n.2944T>C (SLC37A4)
ENST00000638186.1:n.1410T>C (SLC37A4)
ENST00000638360.1:n.1242T>C (SLC37A4)
ENST00000638925.1:n.1375T>C (SLC37A4)
ENST00000650539.1:n.1578T>C (SLC37A4)
ENST00000330775.9:c.1106T>C (SLC37A4)	ENSP00000476242.2:p.Val369Ala
ENST00000357590.9:c.1172T>C (SLC37A4)	ENSP00000476176.2:p.Val391Ala
ENST00000524428.5:n.1342T>C (SLC37A4)
ENST00000525039.5:n.1596T>C (SLC37A4)
ENST00000525102.5:n.1864T>C (SLC37A4)
ENST00000525372.5:n.1204T>C (SLC37A4)
ENST00000526275.5:n.1888T>C (SLC37A4)
ENST00000527992.5:n.1334T>C (SLC37A4)
ENST00000529510.5:n.794T>C (SLC37A4)
ENST00000530407.5:n.1256T>C (SLC37A4)
ENST00000532085.1:n.5124T>C (SLC37A4)
ENST00000533058.5:c.*159A>G (TRAPPC4)	ENSP00000432920.1:n.*159A>G
ENST00000538950.5:c.887T>C (SLC37A4)	ENSP00000475991.2:p.Val296Ala
ENST00000545985.5:c.1106T>C (SLC37A4)	ENSP00000475241.2:p.Val369Ala
NM_001164277.1:c.1106T>C , LRG_187t1:c.1106T>C (SLC37A4)	NP_001157749.1:p.Val369Ala
NM_001164278.1:c.1172T>C (SLC37A4)	NP_001157750.1:p.Val391Ala
NM_001164279.1:c.887T>C (SLC37A4)	NP_001157751.1:p.Val296Ala
NM_001164280.1:c.1106T>C (SLC37A4)	NP_001157752.1:p.Val369Ala
NM_001467.5:c.1106T>C (SLC37A4)	NP_001458.1:p.Val369Ala
NM_001164278.2:c.1172T>C (SLC37A4)	NP_001157750.1:p.Val391Ala
NM_001164279.2:c.887T>C (SLC37A4)	NP_001157751.1:p.Val296Ala
NM_001164280.2:c.1106T>C (SLC37A4)	NP_001157752.1:p.Val369Ala
NM_001467.6:c.1106T>C (SLC37A4)	NP_001458.1:p.Val369Ala
NM_001164277.2:c.1106T>C (SLC37A4) MANE Select	NP_001157749.1:p.Val369Ala