Canonical Allele Identifier: CA382896365

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118896023A>C (hg19) ; chr11:g.119025313A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025313A>C , CM000673.2:g.119025313A>C	GRCh38
NC_000011.9:g.118896023A>C , CM000673.1:g.118896023A>C	GRCh37
NC_000011.8:g.118401233A>C	NCBI36
NG_013331.1:g.10593T>G , LRG_187:g.10593T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1211T>G (SLC37A4)
ENST00000697845.1:n.2200T>G (SLC37A4)
ENST00000697846.1:n.1573T>G (SLC37A4)
ENST00000697847.1:n.1284T>G (SLC37A4)
ENST00000697849.1:n.3677T>G (SLC37A4)
ENST00000697850.1:n.1868T>G (SLC37A4)
ENST00000697851.1:n.2839T>G (SLC37A4)
ENST00000638186.1:n.1305T>G (SLC37A4)
ENST00000638360.1:n.1137T>G (SLC37A4)
ENST00000638925.1:n.1270T>G (SLC37A4)
ENST00000650539.1:n.1473T>G (SLC37A4)
ENST00000330775.9:c.1001T>G (SLC37A4)	ENSP00000476242.2:p.Leu334Trp
ENST00000357590.9:c.1067T>G (SLC37A4)	ENSP00000476176.2:p.Leu356Trp
ENST00000524428.5:n.1237T>G (SLC37A4)
ENST00000525039.5:n.1491T>G (SLC37A4)
ENST00000525102.5:n.1759T>G (SLC37A4)
ENST00000525372.5:n.1099T>G (SLC37A4)
ENST00000526275.5:n.1783T>G (SLC37A4)
ENST00000527992.5:n.1229T>G (SLC37A4)
ENST00000529510.5:n.689T>G (SLC37A4)
ENST00000530407.5:n.1151T>G (SLC37A4)
ENST00000532085.1:n.5019T>G (SLC37A4)
ENST00000533058.5:c.*264A>C (TRAPPC4)	ENSP00000432920.1:n.*264A>C
ENST00000538950.5:c.782T>G (SLC37A4)	ENSP00000475991.2:p.Leu261Trp
ENST00000545985.5:c.1001T>G (SLC37A4)	ENSP00000475241.2:p.Leu334Trp
NM_001164277.1:c.1001T>G , LRG_187t1:c.1001T>G (SLC37A4)	NP_001157749.1:p.Leu334Trp
NM_001164278.1:c.1067T>G (SLC37A4)	NP_001157750.1:p.Leu356Trp
NM_001164279.1:c.782T>G (SLC37A4)	NP_001157751.1:p.Leu261Trp
NM_001164280.1:c.1001T>G (SLC37A4)	NP_001157752.1:p.Leu334Trp
NM_001467.5:c.1001T>G (SLC37A4)	NP_001458.1:p.Leu334Trp
NM_001164278.2:c.1067T>G (SLC37A4)	NP_001157750.1:p.Leu356Trp
NM_001164279.2:c.782T>G (SLC37A4)	NP_001157751.1:p.Leu261Trp
NM_001164280.2:c.1001T>G (SLC37A4)	NP_001157752.1:p.Leu334Trp
NM_001467.6:c.1001T>G (SLC37A4)	NP_001458.1:p.Leu334Trp
NM_001164277.2:c.1001T>G (SLC37A4) MANE Select	NP_001157749.1:p.Leu334Trp