Canonical Allele Identifier: CA382896210

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118896003A>T (hg19) ; chr11:g.119025293A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025293A>T , CM000673.2:g.119025293A>T	GRCh38
NC_000011.9:g.118896003A>T , CM000673.1:g.118896003A>T	GRCh37
NC_000011.8:g.118401213A>T	NCBI36
NG_013331.1:g.10613T>A , LRG_187:g.10613T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1231T>A (SLC37A4)
ENST00000697845.1:n.2220T>A (SLC37A4)
ENST00000697846.1:n.1593T>A (SLC37A4)
ENST00000697847.1:n.1304T>A (SLC37A4)
ENST00000697849.1:n.3697T>A (SLC37A4)
ENST00000697850.1:n.1888T>A (SLC37A4)
ENST00000697851.1:n.2859T>A (SLC37A4)
ENST00000638186.1:n.1325T>A (SLC37A4)
ENST00000638360.1:n.1157T>A (SLC37A4)
ENST00000638925.1:n.1290T>A (SLC37A4)
ENST00000650539.1:n.1493T>A (SLC37A4)
ENST00000330775.9:c.1021T>A (SLC37A4)	ENSP00000476242.2:p.Ser341Thr
ENST00000357590.9:c.1087T>A (SLC37A4)	ENSP00000476176.2:p.Ser363Thr
ENST00000524428.5:n.1257T>A (SLC37A4)
ENST00000525039.5:n.1511T>A (SLC37A4)
ENST00000525102.5:n.1779T>A (SLC37A4)
ENST00000525372.5:n.1119T>A (SLC37A4)
ENST00000526275.5:n.1803T>A (SLC37A4)
ENST00000527992.5:n.1249T>A (SLC37A4)
ENST00000529510.5:n.709T>A (SLC37A4)
ENST00000530407.5:n.1171T>A (SLC37A4)
ENST00000532085.1:n.5039T>A (SLC37A4)
ENST00000533058.5:c.*244A>T (TRAPPC4)	ENSP00000432920.1:n.*244A>T
ENST00000538950.5:c.802T>A (SLC37A4)	ENSP00000475991.2:p.Ser268Thr
ENST00000545985.5:c.1021T>A (SLC37A4)	ENSP00000475241.2:p.Ser341Thr
NM_001164277.1:c.1021T>A , LRG_187t1:c.1021T>A (SLC37A4)	NP_001157749.1:p.Ser341Thr
NM_001164278.1:c.1087T>A (SLC37A4)	NP_001157750.1:p.Ser363Thr
NM_001164279.1:c.802T>A (SLC37A4)	NP_001157751.1:p.Ser268Thr
NM_001164280.1:c.1021T>A (SLC37A4)	NP_001157752.1:p.Ser341Thr
NM_001467.5:c.1021T>A (SLC37A4)	NP_001458.1:p.Ser341Thr
NM_001164278.2:c.1087T>A (SLC37A4)	NP_001157750.1:p.Ser363Thr
NM_001164279.2:c.802T>A (SLC37A4)	NP_001157751.1:p.Ser268Thr
NM_001164280.2:c.1021T>A (SLC37A4)	NP_001157752.1:p.Ser341Thr
NM_001467.6:c.1021T>A (SLC37A4)	NP_001458.1:p.Ser341Thr
NM_001164277.2:c.1021T>A (SLC37A4) MANE Select	NP_001157749.1:p.Ser341Thr