Canonical Allele Identifier: CA2003749669
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027683T= , CM000673.2:g.119027683T= GRCh38
NC_000011.9:g.118898393T= , CM000673.1:g.118898393T= GRCh37
NC_000011.8:g.118403603T= NCBI36
NG_013331.1:g.8223A= , LRG_187:g.8223A=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.800A=
ENST00000697845.1:n.724A=
ENST00000697846.1:n.800A=
ENST00000697847.1:n.800A=
ENST00000697848.1:n.800A=
ENST00000697849.1:n.1839A=
ENST00000697850.1:n.800A=
ENST00000697851.1:n.2160A=
ENST00000638186.1:n.874A=
ENST00000638360.1:n.706A=
ENST00000638925.1:n.807A=
ENST00000650539.1:n.976A=
ENST00000330775.9:c.570A= ENSP00000476242.2:p.Glu190=
ENST00000357590.9:c.570A= ENSP00000476176.2:p.Glu190=
ENST00000524428.5:n.892A=
ENST00000525039.5:n.994A=
ENST00000525102.5:n.1328A=
ENST00000525372.5:n.571A=
ENST00000526275.5:n.1352A=
ENST00000526626.6:n.533A=
ENST00000527992.5:n.798A=
ENST00000529510.5:n.399+511A=
ENST00000530407.5:n.720A=
ENST00000532085.1:n.3181A=
ENST00000532888.6:n.866A=
ENST00000538950.5:c.351A= ENSP00000475991.2:p.Glu117=
ENST00000545985.5:c.570A= ENSP00000475241.2:p.Glu190=
NM_001164277.1:c.570A= , LRG_187t1:c.570A= NP_001157749.1:p.Glu190=
NM_001164278.1:c.570A= NP_001157750.1:p.Glu190=
NM_001164279.1:c.351A= NP_001157751.1:p.Glu117=
NM_001164280.1:c.570A= NP_001157752.1:p.Glu190=
NM_001467.5:c.570A= NP_001458.1:p.Glu190=
NM_001164278.2:c.570A= NP_001157750.1:p.Glu190=
NM_001164279.2:c.351A= NP_001157751.1:p.Glu117=
NM_001164280.2:c.570A= NP_001157752.1:p.Glu190=
NM_001467.6:c.570A= NP_001458.1:p.Glu190=
NM_001164277.2:c.570A= MANE Select NP_001157749.1:p.Glu190=