Canonical Allele Identifier: CA382895266

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895916C>T (hg19) ; chr11:g.119025206C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025206C>T , CM000673.2:g.119025206C>T	GRCh38
NC_000011.9:g.118895916C>T , CM000673.1:g.118895916C>T	GRCh37
NC_000011.8:g.118401126C>T	NCBI36
NG_013331.1:g.10700G>A , LRG_187:g.10700G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1318G>A (SLC37A4)
ENST00000697845.1:n.2307G>A (SLC37A4)
ENST00000697846.1:n.1680G>A (SLC37A4)
ENST00000697847.1:n.1391G>A (SLC37A4)
ENST00000697849.1:n.3784G>A (SLC37A4)
ENST00000697850.1:n.1975G>A (SLC37A4)
ENST00000697851.1:n.2946G>A (SLC37A4)
ENST00000638186.1:n.1412G>A (SLC37A4)
ENST00000638360.1:n.1244G>A (SLC37A4)
ENST00000638925.1:n.1377G>A (SLC37A4)
ENST00000650539.1:n.1580G>A (SLC37A4)
ENST00000330775.9:c.1108G>A (SLC37A4)	ENSP00000476242.2:p.Gly370Arg
ENST00000357590.9:c.1174G>A (SLC37A4)	ENSP00000476176.2:p.Gly392Arg
ENST00000524428.5:n.1344G>A (SLC37A4)
ENST00000525039.5:n.1598G>A (SLC37A4)
ENST00000525102.5:n.1866G>A (SLC37A4)
ENST00000525372.5:n.1206G>A (SLC37A4)
ENST00000526275.5:n.1890G>A (SLC37A4)
ENST00000527992.5:n.1336G>A (SLC37A4)
ENST00000529510.5:n.796G>A (SLC37A4)
ENST00000530407.5:n.1258G>A (SLC37A4)
ENST00000532085.1:n.5126G>A (SLC37A4)
ENST00000533058.5:c.*157C>T (TRAPPC4)	ENSP00000432920.1:n.*157C>T
ENST00000538950.5:c.889G>A (SLC37A4)	ENSP00000475991.2:p.Gly297Arg
ENST00000545985.5:c.1108G>A (SLC37A4)	ENSP00000475241.2:p.Gly370Arg
NM_001164277.1:c.1108G>A , LRG_187t1:c.1108G>A (SLC37A4)	NP_001157749.1:p.Gly370Arg
NM_001164278.1:c.1174G>A (SLC37A4)	NP_001157750.1:p.Gly392Arg
NM_001164279.1:c.889G>A (SLC37A4)	NP_001157751.1:p.Gly297Arg
NM_001164280.1:c.1108G>A (SLC37A4)	NP_001157752.1:p.Gly370Arg
NM_001467.5:c.1108G>A (SLC37A4)	NP_001458.1:p.Gly370Arg
NM_001164278.2:c.1174G>A (SLC37A4)	NP_001157750.1:p.Gly392Arg
NM_001164279.2:c.889G>A (SLC37A4)	NP_001157751.1:p.Gly297Arg
NM_001164280.2:c.1108G>A (SLC37A4)	NP_001157752.1:p.Gly370Arg
NM_001467.6:c.1108G>A (SLC37A4)	NP_001458.1:p.Gly370Arg
NM_001164277.2:c.1108G>A (SLC37A4) MANE Select	NP_001157749.1:p.Gly370Arg