Canonical Allele Identifier: CA2003748805
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025967C= , CM000673.2:g.119025967C= GRCh38
NC_000011.9:g.118896677C= , CM000673.1:g.118896677C= GRCh37
NC_000011.8:g.118401887C= NCBI36
NG_013331.1:g.9939G= , LRG_187:g.9939G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1128G=
ENST00000697845.1:n.1908G=
ENST00000697846.1:n.1128G=
ENST00000697847.1:n.1202-210G=
ENST00000697848.1:n.1214G=
ENST00000697849.1:n.3023G=
ENST00000697850.1:n.1214G=
ENST00000697851.1:n.2822G=
ENST00000638186.1:n.1288G=
ENST00000638360.1:n.1120G=
ENST00000638925.1:n.1253G=
ENST00000650539.1:n.1390G=
ENST00000330775.9:c.984G= ENSP00000476242.2:p.Lys328=
ENST00000357590.9:c.984G= ENSP00000476176.2:p.Lys328=
ENST00000524428.5:n.1220G=
ENST00000525039.5:n.1408G=
ENST00000525102.5:n.1742G=
ENST00000525372.5:n.1082G=
ENST00000526275.5:n.1766G=
ENST00000527992.5:n.1212G=
ENST00000529510.5:n.672G=
ENST00000530407.5:n.1134G=
ENST00000532085.1:n.4365G=
ENST00000538950.5:c.765G= ENSP00000475991.2:p.Lys255=
ENST00000545985.5:c.984G= ENSP00000475241.2:p.Lys328=
NM_001164277.1:c.984G= , LRG_187t1:c.984G= NP_001157749.1:p.Lys328=
NM_001164278.1:c.984G= NP_001157750.1:p.Lys328=
NM_001164279.1:c.765G= NP_001157751.1:p.Lys255=
NM_001164280.1:c.984G= NP_001157752.1:p.Lys328=
NM_001467.5:c.984G= NP_001458.1:p.Lys328=
NM_001164278.2:c.984G= NP_001157750.1:p.Lys328=
NM_001164279.2:c.765G= NP_001157751.1:p.Lys255=
NM_001164280.2:c.984G= NP_001157752.1:p.Lys328=
NM_001467.6:c.984G= NP_001458.1:p.Lys328=
NM_001164277.2:c.984G= MANE Select NP_001157749.1:p.Lys328=