Canonical Allele Identifier: CA477367452
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118896025T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025315T>G , CM000673.2:g.119025315T>G GRCh38
NC_000011.9:g.118896025T>G , CM000673.1:g.118896025T>G GRCh37
NC_000011.8:g.118401235T>G NCBI36
NG_013331.1:g.10591A>C , LRG_187:g.10591A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1209A>C (SLC37A4)
ENST00000697845.1:n.2198A>C (SLC37A4)
ENST00000697846.1:n.1571A>C (SLC37A4)
ENST00000697847.1:n.1282A>C (SLC37A4)
ENST00000697849.1:n.3675A>C (SLC37A4)
ENST00000697850.1:n.1866A>C (SLC37A4)
ENST00000697851.1:n.2837A>C (SLC37A4)
ENST00000638186.1:n.1303A>C (SLC37A4)
ENST00000638360.1:n.1135A>C (SLC37A4)
ENST00000638925.1:n.1268A>C (SLC37A4)
ENST00000650539.1:n.1471A>C (SLC37A4)
ENST00000330775.9:c.999A>C (SLC37A4) ENSP00000476242.2:p.Val333=
ENST00000357590.9:c.1065A>C (SLC37A4) ENSP00000476176.2:p.Val355=
ENST00000524428.5:n.1235A>C (SLC37A4)
ENST00000525039.5:n.1489A>C (SLC37A4)
ENST00000525102.5:n.1757A>C (SLC37A4)
ENST00000525372.5:n.1097A>C (SLC37A4)
ENST00000526275.5:n.1781A>C (SLC37A4)
ENST00000527992.5:n.1227A>C (SLC37A4)
ENST00000529510.5:n.687A>C (SLC37A4)
ENST00000530407.5:n.1149A>C (SLC37A4)
ENST00000532085.1:n.5017A>C (SLC37A4)
ENST00000533058.5:c.*266T>G (TRAPPC4) ENSP00000432920.1:n.*266T>G
ENST00000538950.5:c.780A>C (SLC37A4) ENSP00000475991.2:p.Val260=
ENST00000545985.5:c.999A>C (SLC37A4) ENSP00000475241.2:p.Val333=
NM_001164277.1:c.999A>C , LRG_187t1:c.999A>C (SLC37A4) NP_001157749.1:p.Val333=
NM_001164278.1:c.1065A>C (SLC37A4) NP_001157750.1:p.Val355=
NM_001164279.1:c.780A>C (SLC37A4) NP_001157751.1:p.Val260=
NM_001164280.1:c.999A>C (SLC37A4) NP_001157752.1:p.Val333=
NM_001467.5:c.999A>C (SLC37A4) NP_001458.1:p.Val333=
NM_001164278.2:c.1065A>C (SLC37A4) NP_001157750.1:p.Val355=
NM_001164279.2:c.780A>C (SLC37A4) NP_001157751.1:p.Val260=
NM_001164280.2:c.999A>C (SLC37A4) NP_001157752.1:p.Val333=
NM_001467.6:c.999A>C (SLC37A4) NP_001458.1:p.Val333=
NM_001164277.2:c.999A>C (SLC37A4) MANE Select NP_001157749.1:p.Val333=