Canonical Allele Identifier: CA382893058

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895619T>G (hg19) ; chr11:g.119024909T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024909T>G , CM000673.2:g.119024909T>G	GRCh38
NC_000011.9:g.118895619T>G , CM000673.1:g.118895619T>G	GRCh37
NC_000011.8:g.118400829T>G	NCBI36
NG_013331.1:g.10997A>C , LRG_187:g.10997A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1501A>C (SLC37A4)
ENST00000697845.1:n.2490A>C (SLC37A4)
ENST00000697846.1:n.1863A>C (SLC37A4)
ENST00000697847.1:n.1574A>C (SLC37A4)
ENST00000697849.1:n.3967A>C (SLC37A4)
ENST00000697850.1:n.2158A>C (SLC37A4)
ENST00000697851.1:n.3129A>C (SLC37A4)
ENST00000638186.1:n.1595A>C (SLC37A4)
ENST00000638360.1:n.1427A>C (SLC37A4)
ENST00000638925.1:n.1560A>C (SLC37A4)
ENST00000650539.1:n.1763A>C (SLC37A4)
ENST00000330775.9:c.*1A>C (SLC37A4)	ENSP00000476242.2:n.*1A>C
ENST00000357590.9:c.*1A>C (SLC37A4)	ENSP00000476176.2:n.*1A>C
ENST00000525102.5:n.2049A>C (SLC37A4)
ENST00000526275.5:n.2073A>C (SLC37A4)
ENST00000527992.5:n.1519A>C (SLC37A4)
ENST00000530407.5:n.1441A>C (SLC37A4)
ENST00000532085.1:n.5309A>C (SLC37A4)
ENST00000533058.5:c.634T>G (TRAPPC4)	ENSP00000432920.1:p.Phe212Val
ENST00000538950.5:c.*1A>C (SLC37A4)	ENSP00000475991.2:n.*1A>C
ENST00000545985.5:c.*1A>C (SLC37A4)	ENSP00000475241.2:n.*1A>C
NM_001164277.1:c.*1A>C , LRG_187t1:c.*1A>C (SLC37A4)	NP_001157749.1:n.*1A>C
NM_001164278.1:c.*1A>C (SLC37A4)	NP_001157750.1:n.*1A>C
NM_001164279.1:c.*1A>C (SLC37A4)	NP_001157751.1:n.*1A>C
NM_001164280.1:c.*1A>C (SLC37A4)	NP_001157752.1:n.*1A>C
NM_001467.5:c.*1A>C (SLC37A4)	NP_001458.1:n.*1A>C
NM_001164278.2:c.*1A>C (SLC37A4)	NP_001157750.1:n.*1A>C
NM_001164279.2:c.*1A>C (SLC37A4)	NP_001157751.1:n.*1A>C
NM_001164280.2:c.*1A>C (SLC37A4)	NP_001157752.1:n.*1A>C
NM_001467.6:c.*1A>C (SLC37A4)	NP_001458.1:n.*1A>C
NM_001164277.2:c.*1A>C (SLC37A4) MANE Select	NP_001157749.1:n.*1A>C