Canonical Allele Identifier: CA2003776538
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119030438G= , CM000673.2:g.119030438G= GRCh38
NC_000011.9:g.118901148G= , CM000673.1:g.118901148G= GRCh37
NC_000011.8:g.118406358G= NCBI36
NG_013331.1:g.5469C= , LRG_187:g.5469C=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.34+411C=
ENST00000697846.1:n.34+411C=
ENST00000697847.1:n.34+411C=
ENST00000697848.1:n.34+411C=
ENST00000697850.1:n.34+411C=
ENST00000638360.1:n.42+411C=
ENST00000638925.1:n.41+411C=
ENST00000330775.9:c.-196+411C= ENSP00000476242.2:n.-196+411C=
ENST00000357590.9:c.-196+110C= ENSP00000476176.2:n.-196+110C=
ENST00000525039.5:n.228+110C=
ENST00000525102.5:n.356C=
ENST00000527992.5:n.32+411C=
ENST00000530407.5:n.24+411C=
ENST00000532085.1:n.426C=
ENST00000538950.5:c.-345+411C= ENSP00000475991.2:n.-345+411C=
ENST00000545985.5:c.-402C= ENSP00000475241.2:n.-402C=
NM_001164277.1:c.-402C= , LRG_187t1:c.-402C= NP_001157749.1:n.-402C=
NM_001164278.1:c.-196+110C= NP_001157750.1:n.-196+110C=
NM_001164279.1:c.-345+411C= NP_001157751.1:n.-345+411C=
NM_001467.5:c.-196+411C= NP_001458.1:n.-196+411C=
NM_001164278.2:c.-196+110C= NP_001157750.1:n.-196+110C=
NM_001164279.2:c.-345+411C= NP_001157751.1:n.-345+411C=
NM_001467.6:c.-196+411C= NP_001458.1:n.-196+411C=
NM_001164277.2:c.-402C= MANE Select NP_001157749.1:n.-402C=