Canonical Allele Identifier: CA477125789
Gene: SLC37A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118897690G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026980G>A , CM000673.2:g.119026980G>A GRCh38
NC_000011.9:g.118897690G>A , CM000673.1:g.118897690G>A GRCh37
NC_000011.8:g.118402900G>A NCBI36
NG_013331.1:g.8926C>T , LRG_187:g.8926C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.971C>T
ENST00000697845.1:n.895C>T
ENST00000697846.1:n.971C>T
ENST00000697847.1:n.971C>T
ENST00000697848.1:n.971C>T
ENST00000697849.1:n.2010C>T
ENST00000697850.1:n.971C>T
ENST00000697851.1:n.2331C>T
ENST00000638186.1:n.1045C>T
ENST00000638360.1:n.877C>T
ENST00000638925.1:n.978C>T
ENST00000650539.1:n.1147C>T
ENST00000330775.9:c.741C>T ENSP00000476242.2:p.Gly247=
ENST00000357590.9:c.741C>T ENSP00000476176.2:p.Gly247=
ENST00000524428.5:n.1063C>T
ENST00000525039.5:n.1165C>T
ENST00000525102.5:n.1499C>T
ENST00000525372.5:n.742C>T
ENST00000526275.5:n.1523C>T
ENST00000526626.6:n.704C>T
ENST00000527992.5:n.969C>T
ENST00000529510.5:n.515C>T
ENST00000530407.5:n.891C>T
ENST00000532085.1:n.3352C>T
ENST00000532888.6:n.1037C>T
ENST00000538950.5:c.522C>T ENSP00000475991.2:p.Gly174=
ENST00000545985.5:c.741C>T ENSP00000475241.2:p.Gly247=
NM_001164277.1:c.741C>T , LRG_187t1:c.741C>T NP_001157749.1:p.Gly247=
NM_001164278.1:c.741C>T NP_001157750.1:p.Gly247=
NM_001164279.1:c.522C>T NP_001157751.1:p.Gly174=
NM_001164280.1:c.741C>T NP_001157752.1:p.Gly247=
NM_001467.5:c.741C>T NP_001458.1:p.Gly247=
NM_001164278.2:c.741C>T NP_001157750.1:p.Gly247=
NM_001164279.2:c.522C>T NP_001157751.1:p.Gly174=
NM_001164280.2:c.741C>T NP_001157752.1:p.Gly247=
NM_001467.6:c.741C>T NP_001458.1:p.Gly247=
NM_001164277.2:c.741C>T MANE Select NP_001157749.1:p.Gly247=