Canonical Allele Identifier: CA382894305

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895727T>C (hg19) ; chr11:g.119025017T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025017T>C , CM000673.2:g.119025017T>C	GRCh38
NC_000011.9:g.118895727T>C , CM000673.1:g.118895727T>C	GRCh37
NC_000011.8:g.118400937T>C	NCBI36
NG_013331.1:g.10889A>G , LRG_187:g.10889A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1393A>G (SLC37A4)
ENST00000697845.1:n.2382A>G (SLC37A4)
ENST00000697846.1:n.1755A>G (SLC37A4)
ENST00000697847.1:n.1466A>G (SLC37A4)
ENST00000697849.1:n.3859A>G (SLC37A4)
ENST00000697850.1:n.2050A>G (SLC37A4)
ENST00000697851.1:n.3021A>G (SLC37A4)
ENST00000638186.1:n.1487A>G (SLC37A4)
ENST00000638360.1:n.1319A>G (SLC37A4)
ENST00000638925.1:n.1452A>G (SLC37A4)
ENST00000650539.1:n.1655A>G (SLC37A4)
ENST00000330775.9:c.1183A>G (SLC37A4)	ENSP00000476242.2:p.Thr395Ala
ENST00000357590.9:c.1249A>G (SLC37A4)	ENSP00000476176.2:p.Thr417Ala
ENST00000524428.5:n.1419A>G (SLC37A4)
ENST00000525039.5:n.1673A>G (SLC37A4)
ENST00000525102.5:n.1941A>G (SLC37A4)
ENST00000525372.5:n.1281A>G (SLC37A4)
ENST00000526275.5:n.1965A>G (SLC37A4)
ENST00000527992.5:n.1411A>G (SLC37A4)
ENST00000530407.5:n.1333A>G (SLC37A4)
ENST00000532085.1:n.5201A>G (SLC37A4)
ENST00000533058.5:c.742T>C (TRAPPC4)	ENSP00000432920.1:p.Cys248Arg
ENST00000538950.5:c.964A>G (SLC37A4)	ENSP00000475991.2:p.Thr322Ala
ENST00000545985.5:c.1183A>G (SLC37A4)	ENSP00000475241.2:p.Thr395Ala
NM_001164277.1:c.1183A>G , LRG_187t1:c.1183A>G (SLC37A4)	NP_001157749.1:p.Thr395Ala
NM_001164278.1:c.1249A>G (SLC37A4)	NP_001157750.1:p.Thr417Ala
NM_001164279.1:c.964A>G (SLC37A4)	NP_001157751.1:p.Thr322Ala
NM_001164280.1:c.1183A>G (SLC37A4)	NP_001157752.1:p.Thr395Ala
NM_001467.5:c.1183A>G (SLC37A4)	NP_001458.1:p.Thr395Ala
NM_001164278.2:c.1249A>G (SLC37A4)	NP_001157750.1:p.Thr417Ala
NM_001164279.2:c.964A>G (SLC37A4)	NP_001157751.1:p.Thr322Ala
NM_001164280.2:c.1183A>G (SLC37A4)	NP_001157752.1:p.Thr395Ala
NM_001467.6:c.1183A>G (SLC37A4)	NP_001458.1:p.Thr395Ala
NM_001164277.2:c.1183A>G (SLC37A4) MANE Select	NP_001157749.1:p.Thr395Ala