Canonical Allele Identifier: CA382902003
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027661T>C , CM000673.2:g.119027661T>C GRCh38
NC_000011.9:g.118898371T>C , CM000673.1:g.118898371T>C GRCh37
NC_000011.8:g.118403581T>C NCBI36
NG_013331.1:g.8245A>G , LRG_187:g.8245A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.822A>G
ENST00000697845.1:n.746A>G
ENST00000697846.1:n.822A>G
ENST00000697847.1:n.822A>G
ENST00000697848.1:n.822A>G
ENST00000697849.1:n.1861A>G
ENST00000697850.1:n.822A>G
ENST00000697851.1:n.2182A>G
ENST00000638186.1:n.896A>G
ENST00000638360.1:n.728A>G
ENST00000638925.1:n.829A>G
ENST00000650539.1:n.998A>G
ENST00000330775.9:c.592A>G ENSP00000476242.2:p.Asn198Asp
ENST00000357590.9:c.592A>G ENSP00000476176.2:p.Asn198Asp
ENST00000524428.5:n.914A>G
ENST00000525039.5:n.1016A>G
ENST00000525102.5:n.1350A>G
ENST00000525372.5:n.593A>G
ENST00000526275.5:n.1374A>G
ENST00000526626.6:n.555A>G
ENST00000527992.5:n.820A>G
ENST00000529510.5:n.399+533A>G
ENST00000530407.5:n.742A>G
ENST00000532085.1:n.3203A>G
ENST00000532888.6:n.888A>G
ENST00000538950.5:c.373A>G ENSP00000475991.2:p.Asn125Asp
ENST00000545985.5:c.592A>G ENSP00000475241.2:p.Asn198Asp
NM_001164277.1:c.592A>G , LRG_187t1:c.592A>G NP_001157749.1:p.Asn198Asp
NM_001164278.1:c.592A>G NP_001157750.1:p.Asn198Asp
NM_001164279.1:c.373A>G NP_001157751.1:p.Asn125Asp
NM_001164280.1:c.592A>G NP_001157752.1:p.Asn198Asp
NM_001467.5:c.592A>G NP_001458.1:p.Asn198Asp
NM_001164278.2:c.592A>G NP_001157750.1:p.Asn198Asp
NM_001164279.2:c.373A>G NP_001157751.1:p.Asn125Asp
NM_001164280.2:c.592A>G NP_001157752.1:p.Asn198Asp
NM_001467.6:c.592A>G NP_001458.1:p.Asn198Asp
NM_001164277.2:c.592A>G MANE Select NP_001157749.1:p.Asn198Asp