Canonical Allele Identifier: CA382895656
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025241G>T , CM000673.2:g.119025241G>T GRCh38
NC_000011.9:g.118895951G>T , CM000673.1:g.118895951G>T GRCh37
NC_000011.8:g.118401161G>T NCBI36
NG_013331.1:g.10665C>A , LRG_187:g.10665C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1283C>A (SLC37A4)
ENST00000697845.1:n.2272C>A (SLC37A4)
ENST00000697846.1:n.1645C>A (SLC37A4)
ENST00000697847.1:n.1356C>A (SLC37A4)
ENST00000697849.1:n.3749C>A (SLC37A4)
ENST00000697850.1:n.1940C>A (SLC37A4)
ENST00000697851.1:n.2911C>A (SLC37A4)
ENST00000638186.1:n.1377C>A (SLC37A4)
ENST00000638360.1:n.1209C>A (SLC37A4)
ENST00000638925.1:n.1342C>A (SLC37A4)
ENST00000650539.1:n.1545C>A (SLC37A4)
ENST00000330775.9:c.1073C>A (SLC37A4) ENSP00000476242.2:p.Pro358His
ENST00000357590.9:c.1139C>A (SLC37A4) ENSP00000476176.2:p.Pro380His
ENST00000524428.5:n.1309C>A (SLC37A4)
ENST00000525039.5:n.1563C>A (SLC37A4)
ENST00000525102.5:n.1831C>A (SLC37A4)
ENST00000525372.5:n.1171C>A (SLC37A4)
ENST00000526275.5:n.1855C>A (SLC37A4)
ENST00000527992.5:n.1301C>A (SLC37A4)
ENST00000529510.5:n.761C>A (SLC37A4)
ENST00000530407.5:n.1223C>A (SLC37A4)
ENST00000532085.1:n.5091C>A (SLC37A4)
ENST00000533058.5:c.*192G>T (TRAPPC4) ENSP00000432920.1:n.*192G>T
ENST00000538950.5:c.854C>A (SLC37A4) ENSP00000475991.2:p.Pro285His
ENST00000545985.5:c.1073C>A (SLC37A4) ENSP00000475241.2:p.Pro358His
NM_001164277.1:c.1073C>A , LRG_187t1:c.1073C>A (SLC37A4) NP_001157749.1:p.Pro358His
NM_001164278.1:c.1139C>A (SLC37A4) NP_001157750.1:p.Pro380His
NM_001164279.1:c.854C>A (SLC37A4) NP_001157751.1:p.Pro285His
NM_001164280.1:c.1073C>A (SLC37A4) NP_001157752.1:p.Pro358His
NM_001467.5:c.1073C>A (SLC37A4) NP_001458.1:p.Pro358His
NM_001164278.2:c.1139C>A (SLC37A4) NP_001157750.1:p.Pro380His
NM_001164279.2:c.854C>A (SLC37A4) NP_001157751.1:p.Pro285His
NM_001164280.2:c.1073C>A (SLC37A4) NP_001157752.1:p.Pro358His
NM_001467.6:c.1073C>A (SLC37A4) NP_001458.1:p.Pro358His
NM_001164277.2:c.1073C>A (SLC37A4) MANE Select NP_001157749.1:p.Pro358His