Canonical Allele Identifier: CA2003776470
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119030374G= , CM000673.2:g.119030374G= GRCh38
NC_000011.9:g.118901084G= , CM000673.1:g.118901084G= GRCh37
NC_000011.8:g.118406294G= NCBI36
NG_013331.1:g.5533C= , LRG_187:g.5533C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.34+475C=
ENST00000697846.1:n.34+475C=
ENST00000697847.1:n.34+475C=
ENST00000697848.1:n.34+475C=
ENST00000697850.1:n.34+475C=
ENST00000638360.1:n.42+475C=
ENST00000638925.1:n.41+475C=
ENST00000650539.1:n.6C=
ENST00000330775.9:c.-196+475C= ENSP00000476242.2:n.-196+475C=
ENST00000357590.9:c.-196+174C= ENSP00000476176.2:n.-196+174C=
ENST00000525039.5:n.228+174C=
ENST00000525102.5:n.420C=
ENST00000527992.5:n.32+475C=
ENST00000530407.5:n.24+475C=
ENST00000532085.1:n.490C=
ENST00000538950.5:c.-345+475C= ENSP00000475991.2:n.-345+475C=
ENST00000545985.5:c.-338C= ENSP00000475241.2:n.-338C=
NM_001164277.1:c.-338C= , LRG_187t1:c.-338C= NP_001157749.1:n.-338C=
NM_001164278.1:c.-196+174C= NP_001157750.1:n.-196+174C=
NM_001164279.1:c.-345+475C= NP_001157751.1:n.-345+475C=
NM_001467.5:c.-196+475C= NP_001458.1:n.-196+475C=
NM_001164278.2:c.-196+174C= NP_001157750.1:n.-196+174C=
NM_001164279.2:c.-345+475C= NP_001157751.1:n.-345+475C=
NM_001467.6:c.-196+475C= NP_001458.1:n.-196+475C=
NM_001164277.2:c.-338C= MANE Select NP_001157749.1:n.-338C=