Canonical Allele Identifier: CA382901890
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027643A>T , CM000673.2:g.119027643A>T GRCh38
NC_000011.9:g.118898353A>T , CM000673.1:g.118898353A>T GRCh37
NC_000011.8:g.118403563A>T NCBI36
NG_013331.1:g.8263T>A , LRG_187:g.8263T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.840T>A
ENST00000697845.1:n.764T>A
ENST00000697846.1:n.840T>A
ENST00000697847.1:n.840T>A
ENST00000697848.1:n.840T>A
ENST00000697849.1:n.1879T>A
ENST00000697850.1:n.840T>A
ENST00000697851.1:n.2200T>A
ENST00000638186.1:n.914T>A
ENST00000638360.1:n.746T>A
ENST00000638925.1:n.847T>A
ENST00000650539.1:n.1016T>A
ENST00000330775.9:c.610T>A ENSP00000476242.2:p.Ser204Thr
ENST00000357590.9:c.610T>A ENSP00000476176.2:p.Ser204Thr
ENST00000524428.5:n.932T>A
ENST00000525039.5:n.1034T>A
ENST00000525102.5:n.1368T>A
ENST00000525372.5:n.611T>A
ENST00000526275.5:n.1392T>A
ENST00000526626.6:n.573T>A
ENST00000527992.5:n.838T>A
ENST00000529510.5:n.400-548T>A
ENST00000530407.5:n.760T>A
ENST00000532085.1:n.3221T>A
ENST00000532888.6:n.906T>A
ENST00000538950.5:c.391T>A ENSP00000475991.2:p.Ser131Thr
ENST00000545985.5:c.610T>A ENSP00000475241.2:p.Ser204Thr
NM_001164277.1:c.610T>A , LRG_187t1:c.610T>A NP_001157749.1:p.Ser204Thr
NM_001164278.1:c.610T>A NP_001157750.1:p.Ser204Thr
NM_001164279.1:c.391T>A NP_001157751.1:p.Ser131Thr
NM_001164280.1:c.610T>A NP_001157752.1:p.Ser204Thr
NM_001467.5:c.610T>A NP_001458.1:p.Ser204Thr
NM_001164278.2:c.610T>A NP_001157750.1:p.Ser204Thr
NM_001164279.2:c.391T>A NP_001157751.1:p.Ser131Thr
NM_001164280.2:c.610T>A NP_001157752.1:p.Ser204Thr
NM_001467.6:c.610T>A NP_001458.1:p.Ser204Thr
NM_001164277.2:c.610T>A MANE Select NP_001157749.1:p.Ser204Thr