Canonical Allele Identifier: CA382896345
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

dbSNP Id: rs1326123837

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025310C>A , CM000673.2:g.119025310C>A GRCh38
NC_000011.9:g.118896020C>A , CM000673.1:g.118896020C>A GRCh37
NC_000011.8:g.118401230C>A NCBI36
NG_013331.1:g.10596G>T , LRG_187:g.10596G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1214G>T (SLC37A4)
ENST00000697845.1:n.2203G>T (SLC37A4)
ENST00000697846.1:n.1576G>T (SLC37A4)
ENST00000697847.1:n.1287G>T (SLC37A4)
ENST00000697849.1:n.3680G>T (SLC37A4)
ENST00000697850.1:n.1871G>T (SLC37A4)
ENST00000697851.1:n.2842G>T (SLC37A4)
ENST00000638186.1:n.1308G>T (SLC37A4)
ENST00000638360.1:n.1140G>T (SLC37A4)
ENST00000638925.1:n.1273G>T (SLC37A4)
ENST00000650539.1:n.1476G>T (SLC37A4)
ENST00000330775.9:c.1004G>T (SLC37A4) ENSP00000476242.2:p.Gly335Val
ENST00000357590.9:c.1070G>T (SLC37A4) ENSP00000476176.2:p.Gly357Val
ENST00000524428.5:n.1240G>T (SLC37A4)
ENST00000525039.5:n.1494G>T (SLC37A4)
ENST00000525102.5:n.1762G>T (SLC37A4)
ENST00000525372.5:n.1102G>T (SLC37A4)
ENST00000526275.5:n.1786G>T (SLC37A4)
ENST00000527992.5:n.1232G>T (SLC37A4)
ENST00000529510.5:n.692G>T (SLC37A4)
ENST00000530407.5:n.1154G>T (SLC37A4)
ENST00000532085.1:n.5022G>T (SLC37A4)
ENST00000533058.5:c.*261C>A (TRAPPC4) ENSP00000432920.1:n.*261C>A
ENST00000538950.5:c.785G>T (SLC37A4) ENSP00000475991.2:p.Gly262Val
ENST00000545985.5:c.1004G>T (SLC37A4) ENSP00000475241.2:p.Gly335Val
NM_001164277.1:c.1004G>T , LRG_187t1:c.1004G>T (SLC37A4) NP_001157749.1:p.Gly335Val
NM_001164278.1:c.1070G>T (SLC37A4) NP_001157750.1:p.Gly357Val
NM_001164279.1:c.785G>T (SLC37A4) NP_001157751.1:p.Gly262Val
NM_001164280.1:c.1004G>T (SLC37A4) NP_001157752.1:p.Gly335Val
NM_001467.5:c.1004G>T (SLC37A4) NP_001458.1:p.Gly335Val
NM_001164278.2:c.1070G>T (SLC37A4) NP_001157750.1:p.Gly357Val
NM_001164279.2:c.785G>T (SLC37A4) NP_001157751.1:p.Gly262Val
NM_001164280.2:c.1004G>T (SLC37A4) NP_001157752.1:p.Gly335Val
NM_001467.6:c.1004G>T (SLC37A4) NP_001458.1:p.Gly335Val
NM_001164277.2:c.1004G>T (SLC37A4) MANE Select NP_001157749.1:p.Gly335Val