Canonical Allele Identifier: CA2003749939
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028199G= , CM000673.2:g.119028199G= GRCh38
NC_000011.9:g.118898909G= , CM000673.1:g.118898909G= GRCh37
NC_000011.8:g.118404119G= NCBI36
NG_013331.1:g.7708C= , LRG_187:g.7708C=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.605C=
ENST00000697845.1:n.529C=
ENST00000697846.1:n.605C=
ENST00000697847.1:n.605C=
ENST00000697848.1:n.605C=
ENST00000697849.1:n.1644C=
ENST00000697850.1:n.605C=
ENST00000697851.1:n.1644C=
ENST00000638186.1:n.679C=
ENST00000638360.1:n.613C=
ENST00000638925.1:n.612C=
ENST00000650539.1:n.781C=
ENST00000330775.9:c.376C= ENSP00000476242.2:p.Arg126=
ENST00000357590.9:c.376C= ENSP00000476176.2:p.Arg126=
ENST00000524428.5:n.376C=
ENST00000525039.5:n.799C=
ENST00000525102.5:n.1133C=
ENST00000525372.5:n.376C=
ENST00000525787.1:n.671C=
ENST00000526275.5:n.836C=
ENST00000526626.6:n.344-327C=
ENST00000527992.5:n.603C=
ENST00000529510.5:n.394C=
ENST00000530407.5:n.525C=
ENST00000532085.1:n.2665C=
ENST00000532888.6:n.671C=
ENST00000538950.5:c.157C= ENSP00000475991.2:p.Arg53=
ENST00000545985.5:c.376C= ENSP00000475241.2:p.Arg126=
NM_001164277.1:c.376C= , LRG_187t1:c.376C= NP_001157749.1:p.Arg126=
NM_001164278.1:c.376C= NP_001157750.1:p.Arg126=
NM_001164279.1:c.157C= NP_001157751.1:p.Arg53=
NM_001164280.1:c.376C= NP_001157752.1:p.Arg126=
NM_001467.5:c.376C= NP_001458.1:p.Arg126=
NM_001164278.2:c.376C= NP_001157750.1:p.Arg126=
NM_001164279.2:c.157C= NP_001157751.1:p.Arg53=
NM_001164280.2:c.376C= NP_001157752.1:p.Arg126=
NM_001467.6:c.376C= NP_001458.1:p.Arg126=
NM_001164277.2:c.376C= MANE Select NP_001157749.1:p.Arg126=