Canonical Allele Identifier: CA382894030

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895702A>T (hg19) ; chr11:g.119024992A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024992A>T , CM000673.2:g.119024992A>T	GRCh38
NC_000011.9:g.118895702A>T , CM000673.1:g.118895702A>T	GRCh37
NC_000011.8:g.118400912A>T	NCBI36
NG_013331.1:g.10914T>A , LRG_187:g.10914T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1418T>A (SLC37A4)
ENST00000697845.1:n.2407T>A (SLC37A4)
ENST00000697846.1:n.1780T>A (SLC37A4)
ENST00000697847.1:n.1491T>A (SLC37A4)
ENST00000697849.1:n.3884T>A (SLC37A4)
ENST00000697850.1:n.2075T>A (SLC37A4)
ENST00000697851.1:n.3046T>A (SLC37A4)
ENST00000638186.1:n.1512T>A (SLC37A4)
ENST00000638360.1:n.1344T>A (SLC37A4)
ENST00000638925.1:n.1477T>A (SLC37A4)
ENST00000650539.1:n.1680T>A (SLC37A4)
ENST00000330775.9:c.1208T>A (SLC37A4)	ENSP00000476242.2:p.Ile403Asn
ENST00000357590.9:c.1274T>A (SLC37A4)	ENSP00000476176.2:p.Ile425Asn
ENST00000524428.5:n.1444T>A (SLC37A4)
ENST00000525039.5:n.1698T>A (SLC37A4)
ENST00000525102.5:n.1966T>A (SLC37A4)
ENST00000525372.5:n.1306T>A (SLC37A4)
ENST00000526275.5:n.1990T>A (SLC37A4)
ENST00000527992.5:n.1436T>A (SLC37A4)
ENST00000530407.5:n.1358T>A (SLC37A4)
ENST00000532085.1:n.5226T>A (SLC37A4)
ENST00000533058.5:c.717A>T (TRAPPC4)	ENSP00000432920.1:p.Lys239Asn
ENST00000538950.5:c.989T>A (SLC37A4)	ENSP00000475991.2:p.Ile330Asn
ENST00000545985.5:c.1208T>A (SLC37A4)	ENSP00000475241.2:p.Ile403Asn
NM_001164277.1:c.1208T>A , LRG_187t1:c.1208T>A (SLC37A4)	NP_001157749.1:p.Ile403Asn
NM_001164278.1:c.1274T>A (SLC37A4)	NP_001157750.1:p.Ile425Asn
NM_001164279.1:c.989T>A (SLC37A4)	NP_001157751.1:p.Ile330Asn
NM_001164280.1:c.1208T>A (SLC37A4)	NP_001157752.1:p.Ile403Asn
NM_001467.5:c.1208T>A (SLC37A4)	NP_001458.1:p.Ile403Asn
NM_001164278.2:c.1274T>A (SLC37A4)	NP_001157750.1:p.Ile425Asn
NM_001164279.2:c.989T>A (SLC37A4)	NP_001157751.1:p.Ile330Asn
NM_001164280.2:c.1208T>A (SLC37A4)	NP_001157752.1:p.Ile403Asn
NM_001467.6:c.1208T>A (SLC37A4)	NP_001458.1:p.Ile403Asn
NM_001164277.2:c.1208T>A (SLC37A4) MANE Select	NP_001157749.1:p.Ile403Asn