Canonical Allele Identifier: CA2003775454
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029441A= , CM000673.2:g.119029441A= GRCh38
NC_000011.9:g.118900151A= , CM000673.1:g.118900151A= GRCh37
NC_000011.8:g.118405361A= NCBI36
NG_013331.1:g.6466T= , LRG_187:g.6466T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.158T=
ENST00000697846.1:n.158T=
ENST00000697847.1:n.158T=
ENST00000697848.1:n.158T=
ENST00000697849.1:n.402T=
ENST00000697850.1:n.158T=
ENST00000697851.1:n.402T=
ENST00000638186.1:n.232T=
ENST00000638360.1:n.166T=
ENST00000638925.1:n.165T=
ENST00000650539.1:n.334T=
ENST00000330775.9:c.-72T= ENSP00000476242.2:n.-72T=
ENST00000357590.9:c.-72T= ENSP00000476176.2:n.-72T=
ENST00000525039.5:n.352T=
ENST00000525102.5:n.686T=
ENST00000525787.1:n.224T=
ENST00000526626.6:n.124T=
ENST00000527992.5:n.156T=
ENST00000530407.5:n.148T=
ENST00000532085.1:n.1423T=
ENST00000532888.6:n.124T=
ENST00000534384.1:n.149T=
ENST00000538950.5:c.-221T= ENSP00000475991.2:n.-221T=
ENST00000545985.5:c.-72T= ENSP00000475241.2:n.-72T=
NM_001164277.1:c.-72T= , LRG_187t1:c.-72T= NP_001157749.1:n.-72T=
NM_001164278.1:c.-72T= NP_001157750.1:n.-72T=
NM_001164279.1:c.-221T= NP_001157751.1:n.-221T=
NM_001164280.1:c.-72T= NP_001157752.1:n.-72T=
NM_001467.5:c.-72T= NP_001458.1:n.-72T=
NM_001164278.2:c.-72T= NP_001157750.1:n.-72T=
NM_001164279.2:c.-221T= NP_001157751.1:n.-221T=
NM_001164280.2:c.-72T= NP_001157752.1:n.-72T=
NM_001467.6:c.-72T= NP_001458.1:n.-72T=
NM_001164277.2:c.-72T= MANE Select NP_001157749.1:n.-72T=