Canonical Allele Identifier: CA382893781

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895673G>C (hg19) ; chr11:g.119024963G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024963G>C , CM000673.2:g.119024963G>C	GRCh38
NC_000011.9:g.118895673G>C , CM000673.1:g.118895673G>C	GRCh37
NC_000011.8:g.118400883G>C	NCBI36
NG_013331.1:g.10943C>G , LRG_187:g.10943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1447C>G (SLC37A4)
ENST00000697845.1:n.2436C>G (SLC37A4)
ENST00000697846.1:n.1809C>G (SLC37A4)
ENST00000697847.1:n.1520C>G (SLC37A4)
ENST00000697849.1:n.3913C>G (SLC37A4)
ENST00000697850.1:n.2104C>G (SLC37A4)
ENST00000697851.1:n.3075C>G (SLC37A4)
ENST00000638186.1:n.1541C>G (SLC37A4)
ENST00000638360.1:n.1373C>G (SLC37A4)
ENST00000638925.1:n.1506C>G (SLC37A4)
ENST00000650539.1:n.1709C>G (SLC37A4)
ENST00000330775.9:c.1237C>G (SLC37A4)	ENSP00000476242.2:p.Leu413Val
ENST00000357590.9:c.1303C>G (SLC37A4)	ENSP00000476176.2:p.Leu435Val
ENST00000524428.5:n.1473C>G (SLC37A4)
ENST00000525039.5:n.1727C>G (SLC37A4)
ENST00000525102.5:n.1995C>G (SLC37A4)
ENST00000525372.5:n.1335C>G (SLC37A4)
ENST00000526275.5:n.2019C>G (SLC37A4)
ENST00000527992.5:n.1465C>G (SLC37A4)
ENST00000530407.5:n.1387C>G (SLC37A4)
ENST00000532085.1:n.5255C>G (SLC37A4)
ENST00000533058.5:c.688G>C (TRAPPC4)	ENSP00000432920.1:p.Gly230Arg
ENST00000538950.5:c.1018C>G (SLC37A4)	ENSP00000475991.2:p.Leu340Val
ENST00000545985.5:c.1237C>G (SLC37A4)	ENSP00000475241.2:p.Leu413Val
NM_001164277.1:c.1237C>G , LRG_187t1:c.1237C>G (SLC37A4)	NP_001157749.1:p.Leu413Val
NM_001164278.1:c.1303C>G (SLC37A4)	NP_001157750.1:p.Leu435Val
NM_001164279.1:c.1018C>G (SLC37A4)	NP_001157751.1:p.Leu340Val
NM_001164280.1:c.1237C>G (SLC37A4)	NP_001157752.1:p.Leu413Val
NM_001467.5:c.1237C>G (SLC37A4)	NP_001458.1:p.Leu413Val
NM_001164278.2:c.1303C>G (SLC37A4)	NP_001157750.1:p.Leu435Val
NM_001164279.2:c.1018C>G (SLC37A4)	NP_001157751.1:p.Leu340Val
NM_001164280.2:c.1237C>G (SLC37A4)	NP_001157752.1:p.Leu413Val
NM_001467.6:c.1237C>G (SLC37A4)	NP_001458.1:p.Leu413Val
NM_001164277.2:c.1237C>G (SLC37A4) MANE Select	NP_001157749.1:p.Leu413Val