Canonical Allele Identifier: CA2003749155
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026669G= , CM000673.2:g.119026669G= GRCh38
NC_000011.9:g.118897379G= , CM000673.1:g.118897379G= GRCh37
NC_000011.8:g.118402589G= NCBI36
NG_013331.1:g.9237C= , LRG_187:g.9237C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1014+268C=
ENST00000697845.1:n.1206C=
ENST00000697846.1:n.1014+268C=
ENST00000697847.1:n.1034C=
ENST00000697848.1:n.1034C=
ENST00000697849.1:n.2321C=
ENST00000697850.1:n.1034C=
ENST00000697851.1:n.2642C=
ENST00000638186.1:n.1108C=
ENST00000638360.1:n.940C=
ENST00000638925.1:n.1041C=
ENST00000650539.1:n.1210C=
ENST00000330775.9:c.804C= ENSP00000476242.2:p.Ala268=
ENST00000357590.9:c.804C= ENSP00000476176.2:p.Ala268=
ENST00000524428.5:n.1106+268C=
ENST00000525039.5:n.1228C=
ENST00000525102.5:n.1562C=
ENST00000525372.5:n.805C=
ENST00000526275.5:n.1586C=
ENST00000527992.5:n.1032C=
ENST00000529510.5:n.558+268C=
ENST00000530407.5:n.954C=
ENST00000532085.1:n.3663C=
ENST00000532888.6:n.1348C=
ENST00000538950.5:c.585C= ENSP00000475991.2:p.Ala195=
ENST00000545985.5:c.804C= ENSP00000475241.2:p.Ala268=
NM_001164277.1:c.804C= , LRG_187t1:c.804C= NP_001157749.1:p.Ala268=
NM_001164278.1:c.804C= NP_001157750.1:p.Ala268=
NM_001164279.1:c.585C= NP_001157751.1:p.Ala195=
NM_001164280.1:c.804C= NP_001157752.1:p.Ala268=
NM_001467.5:c.804C= NP_001458.1:p.Ala268=
NM_001164278.2:c.804C= NP_001157750.1:p.Ala268=
NM_001164279.2:c.585C= NP_001157751.1:p.Ala195=
NM_001164280.2:c.804C= NP_001157752.1:p.Ala268=
NM_001467.6:c.804C= NP_001458.1:p.Ala268=
NM_001164277.2:c.804C= MANE Select NP_001157749.1:p.Ala268=