Canonical Allele Identifier: CA2003749370
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027083_119027084delinsTC , CM000673.2:g.119027083_119027084delinsTC GRCh38
NC_000011.9:g.118897793_118897794delinsTC , CM000673.1:g.118897793_118897794delinsTC GRCh37
NC_000011.8:g.118403003_118403004delinsTC NCBI36
NG_013331.1:g.8822_8823delinsGA , LRG_187:g.8822_8823delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.867_868delinsGA
ENST00000697845.1:n.791_792delinsGA
ENST00000697846.1:n.867_868delinsGA
ENST00000697847.1:n.867_868delinsGA
ENST00000697848.1:n.867_868delinsGA
ENST00000697849.1:n.1906_1907delinsGA
ENST00000697850.1:n.867_868delinsGA
ENST00000697851.1:n.2227_2228delinsGA
ENST00000638186.1:n.941_942delinsGA
ENST00000638360.1:n.773_774delinsGA
ENST00000638925.1:n.874_875delinsGA
ENST00000650539.1:n.1043_1044delinsGA
ENST00000330775.9:c.637_638delinsGA ENSP00000476242.2:p.Glu213=
ENST00000357590.9:c.637_638delinsGA ENSP00000476176.2:p.Glu213=
ENST00000524428.5:n.959_960delinsGA
ENST00000525039.5:n.1061_1062delinsGA
ENST00000525102.5:n.1395_1396delinsGA
ENST00000525372.5:n.638_639delinsGA
ENST00000526275.5:n.1419_1420delinsGA
ENST00000526626.6:n.600_601delinsGA
ENST00000527992.5:n.865_866delinsGA
ENST00000529510.5:n.411_412delinsGA
ENST00000530407.5:n.787_788delinsGA
ENST00000532085.1:n.3248_3249delinsGA
ENST00000532888.6:n.933_934delinsGA
ENST00000538950.5:c.418_419delinsGA ENSP00000475991.2:p.Glu140=
ENST00000545985.5:c.637_638delinsGA ENSP00000475241.2:p.Glu213=
NM_001164277.1:c.637_638delinsGA , LRG_187t1:c.637_638delinsGA NP_001157749.1:p.Glu213=
NM_001164278.1:c.637_638delinsGA NP_001157750.1:p.Glu213=
NM_001164279.1:c.418_419delinsGA NP_001157751.1:p.Glu140=
NM_001164280.1:c.637_638delinsGA NP_001157752.1:p.Glu213=
NM_001467.5:c.637_638delinsGA NP_001458.1:p.Glu213=
NM_001164278.2:c.637_638delinsGA NP_001157750.1:p.Glu213=
NM_001164279.2:c.418_419delinsGA NP_001157751.1:p.Glu140=
NM_001164280.2:c.637_638delinsGA NP_001157752.1:p.Glu213=
NM_001467.6:c.637_638delinsGA NP_001458.1:p.Glu213=
NM_001164277.2:c.637_638delinsGA MANE Select NP_001157749.1:p.Glu213=