Canonical Allele Identifier: CA2003774664
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029053G= , CM000673.2:g.119029053G= GRCh38
NC_000011.9:g.118899763G= , CM000673.1:g.118899763G= GRCh37
NC_000011.8:g.118404973G= NCBI36
NG_013331.1:g.6854C= , LRG_187:g.6854C=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.377+169C=
ENST00000697846.1:n.377+169C=
ENST00000697847.1:n.377+169C=
ENST00000697848.1:n.377+169C=
ENST00000697849.1:n.790C=
ENST00000697850.1:n.377+169C=
ENST00000697851.1:n.790C=
ENST00000638186.1:n.451+169C=
ENST00000638360.1:n.385+169C=
ENST00000638925.1:n.384+169C=
ENST00000650539.1:n.553+169C=
ENST00000330775.9:c.148+169C= ENSP00000476242.2:n.148+169C=
ENST00000357590.9:c.148+169C= ENSP00000476176.2:n.148+169C=
ENST00000524428.5:n.148+169C=
ENST00000525039.5:n.571+169C=
ENST00000525102.5:n.905+169C=
ENST00000525372.5:n.148+169C=
ENST00000525787.1:n.443+169C=
ENST00000526626.6:n.343+169C=
ENST00000527992.5:n.375+169C=
ENST00000529510.5:n.166+169C=
ENST00000530407.5:n.198-219C=
ENST00000532085.1:n.1811C=
ENST00000532888.6:n.343+169C=
ENST00000534384.1:n.368+169C=
ENST00000538950.5:c.-171-219C= ENSP00000475991.2:n.-171-219C=
ENST00000545985.5:c.148+169C= ENSP00000475241.2:n.148+169C=
NM_001164277.1:c.148+169C= , LRG_187t1:c.148+169C= NP_001157749.1:n.148+169C=
NM_001164278.1:c.148+169C= NP_001157750.1:n.148+169C=
NM_001164279.1:c.-171-219C= NP_001157751.1:n.-171-219C=
NM_001164280.1:c.148+169C= NP_001157752.1:n.148+169C=
NM_001467.5:c.148+169C= NP_001458.1:n.148+169C=
NM_001164278.2:c.148+169C= NP_001157750.1:n.148+169C=
NM_001164279.2:c.-171-219C= NP_001157751.1:n.-171-219C=
NM_001164280.2:c.148+169C= NP_001157752.1:n.148+169C=
NM_001467.6:c.148+169C= NP_001458.1:n.148+169C=
NM_001164277.2:c.148+169C= MANE Select NP_001157749.1:n.148+169C=