Canonical Allele Identifier: CA382908403
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029275G>C , CM000673.2:g.119029275G>C GRCh38
NC_000011.9:g.118899985G>C , CM000673.1:g.118899985G>C GRCh37
NC_000011.8:g.118405195G>C NCBI36
NG_013331.1:g.6632C>G , LRG_187:g.6632C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.324C>G
ENST00000697846.1:n.324C>G
ENST00000697847.1:n.324C>G
ENST00000697848.1:n.324C>G
ENST00000697849.1:n.568C>G
ENST00000697850.1:n.324C>G
ENST00000697851.1:n.568C>G
ENST00000638186.1:n.398C>G
ENST00000638360.1:n.332C>G
ENST00000638925.1:n.331C>G
ENST00000650539.1:n.500C>G
ENST00000330775.9:c.95C>G ENSP00000476242.2:p.Ser32Cys
ENST00000357590.9:c.95C>G ENSP00000476176.2:p.Ser32Cys
ENST00000524428.5:n.95C>G
ENST00000525039.5:n.518C>G
ENST00000525102.5:n.852C>G
ENST00000525372.5:n.95C>G
ENST00000525787.1:n.390C>G
ENST00000526626.6:n.290C>G
ENST00000527992.5:n.322C>G
ENST00000529510.5:n.113C>G
ENST00000530407.5:n.197+117C>G
ENST00000532085.1:n.1589C>G
ENST00000532888.6:n.290C>G
ENST00000534384.1:n.315C>G
ENST00000538950.5:c.-172+117C>G ENSP00000475991.2:n.-172+117C>G
ENST00000545985.5:c.95C>G ENSP00000475241.2:p.Ser32Cys
NM_001164277.1:c.95C>G , LRG_187t1:c.95C>G NP_001157749.1:p.Ser32Cys
NM_001164278.1:c.95C>G NP_001157750.1:p.Ser32Cys
NM_001164279.1:c.-172+117C>G NP_001157751.1:n.-172+117C>G
NM_001164280.1:c.95C>G NP_001157752.1:p.Ser32Cys
NM_001467.5:c.95C>G NP_001458.1:p.Ser32Cys
NM_001164278.2:c.95C>G NP_001157750.1:p.Ser32Cys
NM_001164279.2:c.-172+117C>G NP_001157751.1:n.-172+117C>G
NM_001164280.2:c.95C>G NP_001157752.1:p.Ser32Cys
NM_001467.6:c.95C>G NP_001458.1:p.Ser32Cys
NM_001164277.2:c.95C>G MANE Select NP_001157749.1:p.Ser32Cys