Canonical Allele Identifier: CA382895239

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895913G>C (hg19) ; chr11:g.119025203G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025203G>C , CM000673.2:g.119025203G>C	GRCh38
NC_000011.9:g.118895913G>C , CM000673.1:g.118895913G>C	GRCh37
NC_000011.8:g.118401123G>C	NCBI36
NG_013331.1:g.10703C>G , LRG_187:g.10703C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1321C>G (SLC37A4)
ENST00000697845.1:n.2310C>G (SLC37A4)
ENST00000697846.1:n.1683C>G (SLC37A4)
ENST00000697847.1:n.1394C>G (SLC37A4)
ENST00000697849.1:n.3787C>G (SLC37A4)
ENST00000697850.1:n.1978C>G (SLC37A4)
ENST00000697851.1:n.2949C>G (SLC37A4)
ENST00000638186.1:n.1415C>G (SLC37A4)
ENST00000638360.1:n.1247C>G (SLC37A4)
ENST00000638925.1:n.1380C>G (SLC37A4)
ENST00000650539.1:n.1583C>G (SLC37A4)
ENST00000330775.9:c.1111C>G (SLC37A4)	ENSP00000476242.2:p.Leu371Val
ENST00000357590.9:c.1177C>G (SLC37A4)	ENSP00000476176.2:p.Leu393Val
ENST00000524428.5:n.1347C>G (SLC37A4)
ENST00000525039.5:n.1601C>G (SLC37A4)
ENST00000525102.5:n.1869C>G (SLC37A4)
ENST00000525372.5:n.1209C>G (SLC37A4)
ENST00000526275.5:n.1893C>G (SLC37A4)
ENST00000527992.5:n.1339C>G (SLC37A4)
ENST00000529510.5:n.799C>G (SLC37A4)
ENST00000530407.5:n.1261C>G (SLC37A4)
ENST00000532085.1:n.5129C>G (SLC37A4)
ENST00000533058.5:c.*154G>C (TRAPPC4)	ENSP00000432920.1:n.*154G>C
ENST00000538950.5:c.892C>G (SLC37A4)	ENSP00000475991.2:p.Leu298Val
ENST00000545985.5:c.1111C>G (SLC37A4)	ENSP00000475241.2:p.Leu371Val
NM_001164277.1:c.1111C>G , LRG_187t1:c.1111C>G (SLC37A4)	NP_001157749.1:p.Leu371Val
NM_001164278.1:c.1177C>G (SLC37A4)	NP_001157750.1:p.Leu393Val
NM_001164279.1:c.892C>G (SLC37A4)	NP_001157751.1:p.Leu298Val
NM_001164280.1:c.1111C>G (SLC37A4)	NP_001157752.1:p.Leu371Val
NM_001467.5:c.1111C>G (SLC37A4)	NP_001458.1:p.Leu371Val
NM_001164278.2:c.1177C>G (SLC37A4)	NP_001157750.1:p.Leu393Val
NM_001164279.2:c.892C>G (SLC37A4)	NP_001157751.1:p.Leu298Val
NM_001164280.2:c.1111C>G (SLC37A4)	NP_001157752.1:p.Leu371Val
NM_001467.6:c.1111C>G (SLC37A4)	NP_001458.1:p.Leu371Val
NM_001164277.2:c.1111C>G (SLC37A4) MANE Select	NP_001157749.1:p.Leu371Val