Canonical Allele Identifier: CA382895312

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895920A>C (hg19) ; chr11:g.119025210A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025210A>C , CM000673.2:g.119025210A>C	GRCh38
NC_000011.9:g.118895920A>C , CM000673.1:g.118895920A>C	GRCh37
NC_000011.8:g.118401130A>C	NCBI36
NG_013331.1:g.10696T>G , LRG_187:g.10696T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1314T>G (SLC37A4)
ENST00000697845.1:n.2303T>G (SLC37A4)
ENST00000697846.1:n.1676T>G (SLC37A4)
ENST00000697847.1:n.1387T>G (SLC37A4)
ENST00000697849.1:n.3780T>G (SLC37A4)
ENST00000697850.1:n.1971T>G (SLC37A4)
ENST00000697851.1:n.2942T>G (SLC37A4)
ENST00000638186.1:n.1408T>G (SLC37A4)
ENST00000638360.1:n.1240T>G (SLC37A4)
ENST00000638925.1:n.1373T>G (SLC37A4)
ENST00000650539.1:n.1576T>G (SLC37A4)
ENST00000330775.9:c.1104T>G (SLC37A4)	ENSP00000476242.2:p.Ile368Met
ENST00000357590.9:c.1170T>G (SLC37A4)	ENSP00000476176.2:p.Ile390Met
ENST00000524428.5:n.1340T>G (SLC37A4)
ENST00000525039.5:n.1594T>G (SLC37A4)
ENST00000525102.5:n.1862T>G (SLC37A4)
ENST00000525372.5:n.1202T>G (SLC37A4)
ENST00000526275.5:n.1886T>G (SLC37A4)
ENST00000527992.5:n.1332T>G (SLC37A4)
ENST00000529510.5:n.792T>G (SLC37A4)
ENST00000530407.5:n.1254T>G (SLC37A4)
ENST00000532085.1:n.5122T>G (SLC37A4)
ENST00000533058.5:c.*161A>C (TRAPPC4)	ENSP00000432920.1:n.*161A>C
ENST00000538950.5:c.885T>G (SLC37A4)	ENSP00000475991.2:p.Ile295Met
ENST00000545985.5:c.1104T>G (SLC37A4)	ENSP00000475241.2:p.Ile368Met
NM_001164277.1:c.1104T>G , LRG_187t1:c.1104T>G (SLC37A4)	NP_001157749.1:p.Ile368Met
NM_001164278.1:c.1170T>G (SLC37A4)	NP_001157750.1:p.Ile390Met
NM_001164279.1:c.885T>G (SLC37A4)	NP_001157751.1:p.Ile295Met
NM_001164280.1:c.1104T>G (SLC37A4)	NP_001157752.1:p.Ile368Met
NM_001467.5:c.1104T>G (SLC37A4)	NP_001458.1:p.Ile368Met
NM_001164278.2:c.1170T>G (SLC37A4)	NP_001157750.1:p.Ile390Met
NM_001164279.2:c.885T>G (SLC37A4)	NP_001157751.1:p.Ile295Met
NM_001164280.2:c.1104T>G (SLC37A4)	NP_001157752.1:p.Ile368Met
NM_001467.6:c.1104T>G (SLC37A4)	NP_001458.1:p.Ile368Met
NM_001164277.2:c.1104T>G (SLC37A4) MANE Select	NP_001157749.1:p.Ile368Met