Canonical Allele Identifier: CA382908418
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029276A>T , CM000673.2:g.119029276A>T GRCh38
NC_000011.9:g.118899986A>T , CM000673.1:g.118899986A>T GRCh37
NC_000011.8:g.118405196A>T NCBI36
NG_013331.1:g.6631T>A , LRG_187:g.6631T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.323T>A
ENST00000697846.1:n.323T>A
ENST00000697847.1:n.323T>A
ENST00000697848.1:n.323T>A
ENST00000697849.1:n.567T>A
ENST00000697850.1:n.323T>A
ENST00000697851.1:n.567T>A
ENST00000638186.1:n.397T>A
ENST00000638360.1:n.331T>A
ENST00000638925.1:n.330T>A
ENST00000650539.1:n.499T>A
ENST00000330775.9:c.94T>A ENSP00000476242.2:p.Ser32Thr
ENST00000357590.9:c.94T>A ENSP00000476176.2:p.Ser32Thr
ENST00000524428.5:n.94T>A
ENST00000525039.5:n.517T>A
ENST00000525102.5:n.851T>A
ENST00000525372.5:n.94T>A
ENST00000525787.1:n.389T>A
ENST00000526626.6:n.289T>A
ENST00000527992.5:n.321T>A
ENST00000529510.5:n.112T>A
ENST00000530407.5:n.197+116T>A
ENST00000532085.1:n.1588T>A
ENST00000532888.6:n.289T>A
ENST00000534384.1:n.314T>A
ENST00000538950.5:c.-172+116T>A ENSP00000475991.2:n.-172+116T>A
ENST00000545985.5:c.94T>A ENSP00000475241.2:p.Ser32Thr
NM_001164277.1:c.94T>A , LRG_187t1:c.94T>A NP_001157749.1:p.Ser32Thr
NM_001164278.1:c.94T>A NP_001157750.1:p.Ser32Thr
NM_001164279.1:c.-172+116T>A NP_001157751.1:n.-172+116T>A
NM_001164280.1:c.94T>A NP_001157752.1:p.Ser32Thr
NM_001467.5:c.94T>A NP_001458.1:p.Ser32Thr
NM_001164278.2:c.94T>A NP_001157750.1:p.Ser32Thr
NM_001164279.2:c.-172+116T>A NP_001157751.1:n.-172+116T>A
NM_001164280.2:c.94T>A NP_001157752.1:p.Ser32Thr
NM_001467.6:c.94T>A NP_001458.1:p.Ser32Thr
NM_001164277.2:c.94T>A MANE Select NP_001157749.1:p.Ser32Thr