Canonical Allele Identifier: CA382894540

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895749A>C (hg19) ; chr11:g.119025039A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025039A>C , CM000673.2:g.119025039A>C	GRCh38
NC_000011.9:g.118895749A>C , CM000673.1:g.118895749A>C	GRCh37
NC_000011.8:g.118400959A>C	NCBI36
NG_013331.1:g.10867T>G , LRG_187:g.10867T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1371T>G (SLC37A4)
ENST00000697845.1:n.2360T>G (SLC37A4)
ENST00000697846.1:n.1733T>G (SLC37A4)
ENST00000697847.1:n.1444T>G (SLC37A4)
ENST00000697849.1:n.3837T>G (SLC37A4)
ENST00000697850.1:n.2028T>G (SLC37A4)
ENST00000697851.1:n.2999T>G (SLC37A4)
ENST00000638186.1:n.1465T>G (SLC37A4)
ENST00000638360.1:n.1297T>G (SLC37A4)
ENST00000638925.1:n.1430T>G (SLC37A4)
ENST00000650539.1:n.1633T>G (SLC37A4)
ENST00000330775.9:c.1161T>G (SLC37A4)	ENSP00000476242.2:p.Ile387Met
ENST00000357590.9:c.1227T>G (SLC37A4)	ENSP00000476176.2:p.Ile409Met
ENST00000524428.5:n.1397T>G (SLC37A4)
ENST00000525039.5:n.1651T>G (SLC37A4)
ENST00000525102.5:n.1919T>G (SLC37A4)
ENST00000525372.5:n.1259T>G (SLC37A4)
ENST00000526275.5:n.1943T>G (SLC37A4)
ENST00000527992.5:n.1389T>G (SLC37A4)
ENST00000530407.5:n.1311T>G (SLC37A4)
ENST00000532085.1:n.5179T>G (SLC37A4)
ENST00000533058.5:c.764A>C (TRAPPC4)	ENSP00000432920.1:p.Gln255Pro
ENST00000538950.5:c.942T>G (SLC37A4)	ENSP00000475991.2:p.Ile314Met
ENST00000545985.5:c.1161T>G (SLC37A4)	ENSP00000475241.2:p.Ile387Met
NM_001164277.1:c.1161T>G , LRG_187t1:c.1161T>G (SLC37A4)	NP_001157749.1:p.Ile387Met
NM_001164278.1:c.1227T>G (SLC37A4)	NP_001157750.1:p.Ile409Met
NM_001164279.1:c.942T>G (SLC37A4)	NP_001157751.1:p.Ile314Met
NM_001164280.1:c.1161T>G (SLC37A4)	NP_001157752.1:p.Ile387Met
NM_001467.5:c.1161T>G (SLC37A4)	NP_001458.1:p.Ile387Met
NM_001164278.2:c.1227T>G (SLC37A4)	NP_001157750.1:p.Ile409Met
NM_001164279.2:c.942T>G (SLC37A4)	NP_001157751.1:p.Ile314Met
NM_001164280.2:c.1161T>G (SLC37A4)	NP_001157752.1:p.Ile387Met
NM_001467.6:c.1161T>G (SLC37A4)	NP_001458.1:p.Ile387Met
NM_001164277.2:c.1161T>G (SLC37A4) MANE Select	NP_001157749.1:p.Ile387Met