Canonical Allele Identifier: CA2003749679
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027698C= , CM000673.2:g.119027698C= GRCh38
NC_000011.9:g.118898408C= , CM000673.1:g.118898408C= GRCh37
NC_000011.8:g.118403618C= NCBI36
NG_013331.1:g.8208G= , LRG_187:g.8208G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.785G=
ENST00000697845.1:n.709G=
ENST00000697846.1:n.785G=
ENST00000697847.1:n.785G=
ENST00000697848.1:n.785G=
ENST00000697849.1:n.1824G=
ENST00000697850.1:n.785G=
ENST00000697851.1:n.2145G=
ENST00000638186.1:n.859G=
ENST00000638360.1:n.691G=
ENST00000638925.1:n.792G=
ENST00000650539.1:n.961G=
ENST00000330775.9:c.555G= ENSP00000476242.2:p.Leu185=
ENST00000357590.9:c.555G= ENSP00000476176.2:p.Leu185=
ENST00000524428.5:n.877G=
ENST00000525039.5:n.979G=
ENST00000525102.5:n.1313G=
ENST00000525372.5:n.556G=
ENST00000526275.5:n.1337G=
ENST00000526626.6:n.518G=
ENST00000527992.5:n.783G=
ENST00000529510.5:n.399+496G=
ENST00000530407.5:n.705G=
ENST00000532085.1:n.3166G=
ENST00000532888.6:n.851G=
ENST00000538950.5:c.336G= ENSP00000475991.2:p.Leu112=
ENST00000545985.5:c.555G= ENSP00000475241.2:p.Leu185=
NM_001164277.1:c.555G= , LRG_187t1:c.555G= NP_001157749.1:p.Leu185=
NM_001164278.1:c.555G= NP_001157750.1:p.Leu185=
NM_001164279.1:c.336G= NP_001157751.1:p.Leu112=
NM_001164280.1:c.555G= NP_001157752.1:p.Leu185=
NM_001467.5:c.555G= NP_001458.1:p.Leu185=
NM_001164278.2:c.555G= NP_001157750.1:p.Leu185=
NM_001164279.2:c.336G= NP_001157751.1:p.Leu112=
NM_001164280.2:c.555G= NP_001157752.1:p.Leu185=
NM_001467.6:c.555G= NP_001458.1:p.Leu185=
NM_001164277.2:c.555G= MANE Select NP_001157749.1:p.Leu185=