Canonical Allele Identifier: CA2839456512
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027656dup , CM000673.2:g.119027656dup GRCh38
NC_000011.9:g.118898366dup , CM000673.1:g.118898366dup GRCh37
NC_000011.8:g.118403576dup NCBI36
NG_013331.1:g.8251dup , LRG_187:g.8251dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.828dup
ENST00000697845.1:n.752dup
ENST00000697846.1:n.828dup
ENST00000697847.1:n.828dup
ENST00000697848.1:n.828dup
ENST00000697849.1:n.1867dup
ENST00000697850.1:n.828dup
ENST00000697851.1:n.2188dup
ENST00000638186.1:n.902dup
ENST00000638360.1:n.734dup
ENST00000638925.1:n.835dup
ENST00000650539.1:n.1004dup
ENST00000330775.9:c.598dup ENSP00000476242.2:p.Asp200GlyfsTer6
ENST00000357590.9:c.598dup ENSP00000476176.2:p.Asp200GlyfsTer6
ENST00000524428.5:n.920dup
ENST00000525039.5:n.1022dup
ENST00000525102.5:n.1356dup
ENST00000525372.5:n.599dup
ENST00000526275.5:n.1380dup
ENST00000526626.6:n.561dup
ENST00000527992.5:n.826dup
ENST00000529510.5:n.399+539dup
ENST00000530407.5:n.748dup
ENST00000532085.1:n.3209dup
ENST00000532888.6:n.894dup
ENST00000538950.5:c.379dup ENSP00000475991.2:p.Asp127GlyfsTer6
ENST00000545985.5:c.598dup ENSP00000475241.2:p.Asp200GlyfsTer6
NM_001164277.1:c.598dup , LRG_187t1:c.598dup NP_001157749.1:p.Asp200GlyfsTer6
NM_001164278.1:c.598dup NP_001157750.1:p.Asp200GlyfsTer6
NM_001164279.1:c.379dup NP_001157751.1:p.Asp127GlyfsTer6
NM_001164280.1:c.598dup NP_001157752.1:p.Asp200GlyfsTer6
NM_001467.5:c.598dup NP_001458.1:p.Asp200GlyfsTer6
NM_001164278.2:c.598dup NP_001157750.1:p.Asp200GlyfsTer6
NM_001164279.2:c.379dup NP_001157751.1:p.Asp127GlyfsTer6
NM_001164280.2:c.598dup NP_001157752.1:p.Asp200GlyfsTer6
NM_001467.6:c.598dup NP_001458.1:p.Asp200GlyfsTer6
NM_001164277.2:c.598dup MANE Select NP_001157749.1:p.Asp200GlyfsTer6