Canonical Allele Identifier: CA382894104

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895710A>T (hg19) ; chr11:g.119025000A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025000A>T , CM000673.2:g.119025000A>T	GRCh38
NC_000011.9:g.118895710A>T , CM000673.1:g.118895710A>T	GRCh37
NC_000011.8:g.118400920A>T	NCBI36
NG_013331.1:g.10906T>A , LRG_187:g.10906T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1410T>A (SLC37A4)
ENST00000697845.1:n.2399T>A (SLC37A4)
ENST00000697846.1:n.1772T>A (SLC37A4)
ENST00000697847.1:n.1483T>A (SLC37A4)
ENST00000697849.1:n.3876T>A (SLC37A4)
ENST00000697850.1:n.2067T>A (SLC37A4)
ENST00000697851.1:n.3038T>A (SLC37A4)
ENST00000638186.1:n.1504T>A (SLC37A4)
ENST00000638360.1:n.1336T>A (SLC37A4)
ENST00000638925.1:n.1469T>A (SLC37A4)
ENST00000650539.1:n.1672T>A (SLC37A4)
ENST00000330775.9:c.1200T>A (SLC37A4)	ENSP00000476242.2:p.Ala400=
ENST00000357590.9:c.1266T>A (SLC37A4)	ENSP00000476176.2:p.Ala422=
ENST00000524428.5:n.1436T>A (SLC37A4)
ENST00000525039.5:n.1690T>A (SLC37A4)
ENST00000525102.5:n.1958T>A (SLC37A4)
ENST00000525372.5:n.1298T>A (SLC37A4)
ENST00000526275.5:n.1982T>A (SLC37A4)
ENST00000527992.5:n.1428T>A (SLC37A4)
ENST00000530407.5:n.1350T>A (SLC37A4)
ENST00000532085.1:n.5218T>A (SLC37A4)
ENST00000533058.5:c.725A>T (TRAPPC4)	ENSP00000432920.1:p.Gln242Leu
ENST00000538950.5:c.981T>A (SLC37A4)	ENSP00000475991.2:p.Ala327=
ENST00000545985.5:c.1200T>A (SLC37A4)	ENSP00000475241.2:p.Ala400=
NM_001164277.1:c.1200T>A , LRG_187t1:c.1200T>A (SLC37A4)	NP_001157749.1:p.Ala400=
NM_001164278.1:c.1266T>A (SLC37A4)	NP_001157750.1:p.Ala422=
NM_001164279.1:c.981T>A (SLC37A4)	NP_001157751.1:p.Ala327=
NM_001164280.1:c.1200T>A (SLC37A4)	NP_001157752.1:p.Ala400=
NM_001467.5:c.1200T>A (SLC37A4)	NP_001458.1:p.Ala400=
NM_001164278.2:c.1266T>A (SLC37A4)	NP_001157750.1:p.Ala422=
NM_001164279.2:c.981T>A (SLC37A4)	NP_001157751.1:p.Ala327=
NM_001164280.2:c.1200T>A (SLC37A4)	NP_001157752.1:p.Ala400=
NM_001467.6:c.1200T>A (SLC37A4)	NP_001458.1:p.Ala400=
NM_001164277.2:c.1200T>A (SLC37A4) MANE Select	NP_001157749.1:p.Ala400=