Canonical Allele Identifier: CA2003775300
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029373A= , CM000673.2:g.119029373A= GRCh38
NC_000011.9:g.118900083A= , CM000673.1:g.118900083A= GRCh37
NC_000011.8:g.118405293A= NCBI36
NG_013331.1:g.6534T= , LRG_187:g.6534T=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.226T=
ENST00000697846.1:n.226T=
ENST00000697847.1:n.226T=
ENST00000697848.1:n.226T=
ENST00000697849.1:n.470T=
ENST00000697850.1:n.226T=
ENST00000697851.1:n.470T=
ENST00000638186.1:n.300T=
ENST00000638360.1:n.234T=
ENST00000638925.1:n.233T=
ENST00000650539.1:n.402T=
ENST00000330775.9:c.-4T= ENSP00000476242.2:n.-4T=
ENST00000357590.9:c.-4T= ENSP00000476176.2:n.-4T=
ENST00000525039.5:n.420T=
ENST00000525102.5:n.754T=
ENST00000525787.1:n.292T=
ENST00000526626.6:n.192T=
ENST00000527992.5:n.224T=
ENST00000529510.5:n.15T=
ENST00000530407.5:n.197+19T=
ENST00000532085.1:n.1491T=
ENST00000532888.6:n.192T=
ENST00000534384.1:n.217T=
ENST00000538950.5:c.-172+19T= ENSP00000475991.2:n.-172+19T=
ENST00000545985.5:c.-4T= ENSP00000475241.2:n.-4T=
NM_001164277.1:c.-4T= , LRG_187t1:c.-4T= NP_001157749.1:n.-4T=
NM_001164278.1:c.-4T= NP_001157750.1:n.-4T=
NM_001164279.1:c.-172+19T= NP_001157751.1:n.-172+19T=
NM_001164280.1:c.-4T= NP_001157752.1:n.-4T=
NM_001467.5:c.-4T= NP_001458.1:n.-4T=
NM_001164278.2:c.-4T= NP_001157750.1:n.-4T=
NM_001164279.2:c.-172+19T= NP_001157751.1:n.-172+19T=
NM_001164280.2:c.-4T= NP_001157752.1:n.-4T=
NM_001467.6:c.-4T= NP_001458.1:n.-4T=
NM_001164277.2:c.-4T= MANE Select NP_001157749.1:n.-4T=