Canonical Allele Identifier: CA382894354

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895733A>G (hg19) ; chr11:g.119025023A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025023A>G , CM000673.2:g.119025023A>G	GRCh38
NC_000011.9:g.118895733A>G , CM000673.1:g.118895733A>G	GRCh37
NC_000011.8:g.118400943A>G	NCBI36
NG_013331.1:g.10883T>C , LRG_187:g.10883T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1387T>C (SLC37A4)
ENST00000697845.1:n.2376T>C (SLC37A4)
ENST00000697846.1:n.1749T>C (SLC37A4)
ENST00000697847.1:n.1460T>C (SLC37A4)
ENST00000697849.1:n.3853T>C (SLC37A4)
ENST00000697850.1:n.2044T>C (SLC37A4)
ENST00000697851.1:n.3015T>C (SLC37A4)
ENST00000638186.1:n.1481T>C (SLC37A4)
ENST00000638360.1:n.1313T>C (SLC37A4)
ENST00000638925.1:n.1446T>C (SLC37A4)
ENST00000650539.1:n.1649T>C (SLC37A4)
ENST00000330775.9:c.1177T>C (SLC37A4)	ENSP00000476242.2:p.Trp393Arg
ENST00000357590.9:c.1243T>C (SLC37A4)	ENSP00000476176.2:p.Trp415Arg
ENST00000524428.5:n.1413T>C (SLC37A4)
ENST00000525039.5:n.1667T>C (SLC37A4)
ENST00000525102.5:n.1935T>C (SLC37A4)
ENST00000525372.5:n.1275T>C (SLC37A4)
ENST00000526275.5:n.1959T>C (SLC37A4)
ENST00000527992.5:n.1405T>C (SLC37A4)
ENST00000530407.5:n.1327T>C (SLC37A4)
ENST00000532085.1:n.5195T>C (SLC37A4)
ENST00000533058.5:c.748A>G (TRAPPC4)	ENSP00000432920.1:p.Asn250Asp
ENST00000538950.5:c.958T>C (SLC37A4)	ENSP00000475991.2:p.Trp320Arg
ENST00000545985.5:c.1177T>C (SLC37A4)	ENSP00000475241.2:p.Trp393Arg
NM_001164277.1:c.1177T>C , LRG_187t1:c.1177T>C (SLC37A4)	NP_001157749.1:p.Trp393Arg
NM_001164278.1:c.1243T>C (SLC37A4)	NP_001157750.1:p.Trp415Arg
NM_001164279.1:c.958T>C (SLC37A4)	NP_001157751.1:p.Trp320Arg
NM_001164280.1:c.1177T>C (SLC37A4)	NP_001157752.1:p.Trp393Arg
NM_001467.5:c.1177T>C (SLC37A4)	NP_001458.1:p.Trp393Arg
NM_001164278.2:c.1243T>C (SLC37A4)	NP_001157750.1:p.Trp415Arg
NM_001164279.2:c.958T>C (SLC37A4)	NP_001157751.1:p.Trp320Arg
NM_001164280.2:c.1177T>C (SLC37A4)	NP_001157752.1:p.Trp393Arg
NM_001467.6:c.1177T>C (SLC37A4)	NP_001458.1:p.Trp393Arg
NM_001164277.2:c.1177T>C (SLC37A4) MANE Select	NP_001157749.1:p.Trp393Arg