Canonical Allele Identifier: CA2003749322
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026982C= , CM000673.2:g.119026982C= GRCh38
NC_000011.9:g.118897692C= , CM000673.1:g.118897692C= GRCh37
NC_000011.8:g.118402902C= NCBI36
NG_013331.1:g.8924G= , LRG_187:g.8924G=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.969G=
ENST00000697845.1:n.893G=
ENST00000697846.1:n.969G=
ENST00000697847.1:n.969G=
ENST00000697848.1:n.969G=
ENST00000697849.1:n.2008G=
ENST00000697850.1:n.969G=
ENST00000697851.1:n.2329G=
ENST00000638186.1:n.1043G=
ENST00000638360.1:n.875G=
ENST00000638925.1:n.976G=
ENST00000650539.1:n.1145G=
ENST00000330775.9:c.739G= ENSP00000476242.2:p.Gly247=
ENST00000357590.9:c.739G= ENSP00000476176.2:p.Gly247=
ENST00000524428.5:n.1061G=
ENST00000525039.5:n.1163G=
ENST00000525102.5:n.1497G=
ENST00000525372.5:n.740G=
ENST00000526275.5:n.1521G=
ENST00000526626.6:n.702G=
ENST00000527992.5:n.967G=
ENST00000529510.5:n.513G=
ENST00000530407.5:n.889G=
ENST00000532085.1:n.3350G=
ENST00000532888.6:n.1035G=
ENST00000538950.5:c.520G= ENSP00000475991.2:p.Gly174=
ENST00000545985.5:c.739G= ENSP00000475241.2:p.Gly247=
NM_001164277.1:c.739G= , LRG_187t1:c.739G= NP_001157749.1:p.Gly247=
NM_001164278.1:c.739G= NP_001157750.1:p.Gly247=
NM_001164279.1:c.520G= NP_001157751.1:p.Gly174=
NM_001164280.1:c.739G= NP_001157752.1:p.Gly247=
NM_001467.5:c.739G= NP_001458.1:p.Gly247=
NM_001164278.2:c.739G= NP_001157750.1:p.Gly247=
NM_001164279.2:c.520G= NP_001157751.1:p.Gly174=
NM_001164280.2:c.739G= NP_001157752.1:p.Gly247=
NM_001467.6:c.739G= NP_001458.1:p.Gly247=
NM_001164277.2:c.739G= MANE Select NP_001157749.1:p.Gly247=