Canonical Allele Identifier: CA2003749903
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028136C= , CM000673.2:g.119028136C= GRCh38
NC_000011.9:g.118898846C= , CM000673.1:g.118898846C= GRCh37
NC_000011.8:g.118404056C= NCBI36
NG_013331.1:g.7771G= , LRG_187:g.7771G=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.610+58G=
ENST00000697845.1:n.534+58G=
ENST00000697846.1:n.610+58G=
ENST00000697847.1:n.610+58G=
ENST00000697848.1:n.610+58G=
ENST00000697849.1:n.1649+58G=
ENST00000697850.1:n.610+58G=
ENST00000697851.1:n.1707G=
ENST00000638186.1:n.684+58G=
ENST00000638360.1:n.618+58G=
ENST00000638925.1:n.617+58G=
ENST00000650539.1:n.786+58G=
ENST00000330775.9:c.381+58G= ENSP00000476242.2:n.381+58G=
ENST00000357590.9:c.381+58G= ENSP00000476176.2:n.381+58G=
ENST00000524428.5:n.439G=
ENST00000525039.5:n.804+58G=
ENST00000525102.5:n.1138+58G=
ENST00000525372.5:n.381+58G=
ENST00000525787.1:n.734G=
ENST00000526275.5:n.899G=
ENST00000526626.6:n.344-264G=
ENST00000527992.5:n.608+58G=
ENST00000529510.5:n.399+58G=
ENST00000530407.5:n.530+58G=
ENST00000532085.1:n.2728G=
ENST00000532888.6:n.676+58G=
ENST00000538950.5:c.162+58G= ENSP00000475991.2:n.162+58G=
ENST00000545985.5:c.381+58G= ENSP00000475241.2:n.381+58G=
NM_001164277.1:c.381+58G= , LRG_187t1:c.381+58G= NP_001157749.1:n.381+58G=
NM_001164278.1:c.381+58G= NP_001157750.1:n.381+58G=
NM_001164279.1:c.162+58G= NP_001157751.1:n.162+58G=
NM_001164280.1:c.381+58G= NP_001157752.1:n.381+58G=
NM_001467.5:c.381+58G= NP_001458.1:n.381+58G=
NM_001164278.2:c.381+58G= NP_001157750.1:n.381+58G=
NM_001164279.2:c.162+58G= NP_001157751.1:n.162+58G=
NM_001164280.2:c.381+58G= NP_001157752.1:n.381+58G=
NM_001467.6:c.381+58G= NP_001458.1:n.381+58G=
NM_001164277.2:c.381+58G= MANE Select NP_001157749.1:n.381+58G=