Canonical Allele Identifier: CA477367353
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118895968T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025258T>A , CM000673.2:g.119025258T>A GRCh38
NC_000011.9:g.118895968T>A , CM000673.1:g.118895968T>A GRCh37
NC_000011.8:g.118401178T>A NCBI36
NG_013331.1:g.10648A>T , LRG_187:g.10648A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1266A>T (SLC37A4)
ENST00000697845.1:n.2255A>T (SLC37A4)
ENST00000697846.1:n.1628A>T (SLC37A4)
ENST00000697847.1:n.1339A>T (SLC37A4)
ENST00000697849.1:n.3732A>T (SLC37A4)
ENST00000697850.1:n.1923A>T (SLC37A4)
ENST00000697851.1:n.2894A>T (SLC37A4)
ENST00000638186.1:n.1360A>T (SLC37A4)
ENST00000638360.1:n.1192A>T (SLC37A4)
ENST00000638925.1:n.1325A>T (SLC37A4)
ENST00000650539.1:n.1528A>T (SLC37A4)
ENST00000330775.9:c.1056A>T (SLC37A4) ENSP00000476242.2:p.Ile352=
ENST00000357590.9:c.1122A>T (SLC37A4) ENSP00000476176.2:p.Ile374=
ENST00000524428.5:n.1292A>T (SLC37A4)
ENST00000525039.5:n.1546A>T (SLC37A4)
ENST00000525102.5:n.1814A>T (SLC37A4)
ENST00000525372.5:n.1154A>T (SLC37A4)
ENST00000526275.5:n.1838A>T (SLC37A4)
ENST00000527992.5:n.1284A>T (SLC37A4)
ENST00000529510.5:n.744A>T (SLC37A4)
ENST00000530407.5:n.1206A>T (SLC37A4)
ENST00000532085.1:n.5074A>T (SLC37A4)
ENST00000533058.5:c.*209T>A (TRAPPC4) ENSP00000432920.1:n.*209T>A
ENST00000538950.5:c.837A>T (SLC37A4) ENSP00000475991.2:p.Ile279=
ENST00000545985.5:c.1056A>T (SLC37A4) ENSP00000475241.2:p.Ile352=
NM_001164277.1:c.1056A>T , LRG_187t1:c.1056A>T (SLC37A4) NP_001157749.1:p.Ile352=
NM_001164278.1:c.1122A>T (SLC37A4) NP_001157750.1:p.Ile374=
NM_001164279.1:c.837A>T (SLC37A4) NP_001157751.1:p.Ile279=
NM_001164280.1:c.1056A>T (SLC37A4) NP_001157752.1:p.Ile352=
NM_001467.5:c.1056A>T (SLC37A4) NP_001458.1:p.Ile352=
NM_001164278.2:c.1122A>T (SLC37A4) NP_001157750.1:p.Ile374=
NM_001164279.2:c.837A>T (SLC37A4) NP_001157751.1:p.Ile279=
NM_001164280.2:c.1056A>T (SLC37A4) NP_001157752.1:p.Ile352=
NM_001467.6:c.1056A>T (SLC37A4) NP_001458.1:p.Ile352=
NM_001164277.2:c.1056A>T (SLC37A4) MANE Select NP_001157749.1:p.Ile352=