Canonical Allele Identifier: CA2003749652
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027653G= , CM000673.2:g.119027653G= GRCh38
NC_000011.9:g.118898363G= , CM000673.1:g.118898363G= GRCh37
NC_000011.8:g.118403573G= NCBI36
NG_013331.1:g.8253C= , LRG_187:g.8253C=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.830C=
ENST00000697845.1:n.754C=
ENST00000697846.1:n.830C=
ENST00000697847.1:n.830C=
ENST00000697848.1:n.830C=
ENST00000697849.1:n.1869C=
ENST00000697850.1:n.830C=
ENST00000697851.1:n.2190C=
ENST00000638186.1:n.904C=
ENST00000638360.1:n.736C=
ENST00000638925.1:n.837C=
ENST00000650539.1:n.1006C=
ENST00000330775.9:c.600C= ENSP00000476242.2:p.Asp200=
ENST00000357590.9:c.600C= ENSP00000476176.2:p.Asp200=
ENST00000524428.5:n.922C=
ENST00000525039.5:n.1024C=
ENST00000525102.5:n.1358C=
ENST00000525372.5:n.601C=
ENST00000526275.5:n.1382C=
ENST00000526626.6:n.563C=
ENST00000527992.5:n.828C=
ENST00000529510.5:n.399+541C=
ENST00000530407.5:n.750C=
ENST00000532085.1:n.3211C=
ENST00000532888.6:n.896C=
ENST00000538950.5:c.381C= ENSP00000475991.2:p.Asp127=
ENST00000545985.5:c.600C= ENSP00000475241.2:p.Asp200=
NM_001164277.1:c.600C= , LRG_187t1:c.600C= NP_001157749.1:p.Asp200=
NM_001164278.1:c.600C= NP_001157750.1:p.Asp200=
NM_001164279.1:c.381C= NP_001157751.1:p.Asp127=
NM_001164280.1:c.600C= NP_001157752.1:p.Asp200=
NM_001467.5:c.600C= NP_001458.1:p.Asp200=
NM_001164278.2:c.600C= NP_001157750.1:p.Asp200=
NM_001164279.2:c.381C= NP_001157751.1:p.Asp127=
NM_001164280.2:c.600C= NP_001157752.1:p.Asp200=
NM_001467.6:c.600C= NP_001458.1:p.Asp200=
NM_001164277.2:c.600C= MANE Select NP_001157749.1:p.Asp200=