Canonical Allele Identifier: CA382894246

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895721A>G (hg19) ; chr11:g.119025011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025011A>G , CM000673.2:g.119025011A>G	GRCh38
NC_000011.9:g.118895721A>G , CM000673.1:g.118895721A>G	GRCh37
NC_000011.8:g.118400931A>G	NCBI36
NG_013331.1:g.10895T>C , LRG_187:g.10895T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1399T>C (SLC37A4)
ENST00000697845.1:n.2388T>C (SLC37A4)
ENST00000697846.1:n.1761T>C (SLC37A4)
ENST00000697847.1:n.1472T>C (SLC37A4)
ENST00000697849.1:n.3865T>C (SLC37A4)
ENST00000697850.1:n.2056T>C (SLC37A4)
ENST00000697851.1:n.3027T>C (SLC37A4)
ENST00000638186.1:n.1493T>C (SLC37A4)
ENST00000638360.1:n.1325T>C (SLC37A4)
ENST00000638925.1:n.1458T>C (SLC37A4)
ENST00000650539.1:n.1661T>C (SLC37A4)
ENST00000330775.9:c.1189T>C (SLC37A4)	ENSP00000476242.2:p.Phe397Leu
ENST00000357590.9:c.1255T>C (SLC37A4)	ENSP00000476176.2:p.Phe419Leu
ENST00000524428.5:n.1425T>C (SLC37A4)
ENST00000525039.5:n.1679T>C (SLC37A4)
ENST00000525102.5:n.1947T>C (SLC37A4)
ENST00000525372.5:n.1287T>C (SLC37A4)
ENST00000526275.5:n.1971T>C (SLC37A4)
ENST00000527992.5:n.1417T>C (SLC37A4)
ENST00000530407.5:n.1339T>C (SLC37A4)
ENST00000532085.1:n.5207T>C (SLC37A4)
ENST00000533058.5:c.736A>G (TRAPPC4)	ENSP00000432920.1:p.Arg246Gly
ENST00000538950.5:c.970T>C (SLC37A4)	ENSP00000475991.2:p.Phe324Leu
ENST00000545985.5:c.1189T>C (SLC37A4)	ENSP00000475241.2:p.Phe397Leu
NM_001164277.1:c.1189T>C , LRG_187t1:c.1189T>C (SLC37A4)	NP_001157749.1:p.Phe397Leu
NM_001164278.1:c.1255T>C (SLC37A4)	NP_001157750.1:p.Phe419Leu
NM_001164279.1:c.970T>C (SLC37A4)	NP_001157751.1:p.Phe324Leu
NM_001164280.1:c.1189T>C (SLC37A4)	NP_001157752.1:p.Phe397Leu
NM_001467.5:c.1189T>C (SLC37A4)	NP_001458.1:p.Phe397Leu
NM_001164278.2:c.1255T>C (SLC37A4)	NP_001157750.1:p.Phe419Leu
NM_001164279.2:c.970T>C (SLC37A4)	NP_001157751.1:p.Phe324Leu
NM_001164280.2:c.1189T>C (SLC37A4)	NP_001157752.1:p.Phe397Leu
NM_001467.6:c.1189T>C (SLC37A4)	NP_001458.1:p.Phe397Leu
NM_001164277.2:c.1189T>C (SLC37A4) MANE Select	NP_001157749.1:p.Phe397Leu