Canonical Allele Identifier: CA2616341051
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029720del , CM000673.2:g.119029720del GRCh38
NC_000011.9:g.118900430del , CM000673.1:g.118900430del GRCh37
NC_000011.8:g.118405640del NCBI36
NG_013331.1:g.6188del , LRG_187:g.6188del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-155del
ENST00000697846.1:n.35-155del
ENST00000697847.1:n.35-155del
ENST00000697848.1:n.35-155del
ENST00000697849.1:n.124del
ENST00000697850.1:n.35-155del
ENST00000697851.1:n.124del
ENST00000638186.1:n.108+148del
ENST00000638360.1:n.43-155del
ENST00000638925.1:n.42-155del
ENST00000650539.1:n.211-155del
ENST00000330775.9:c.-195-155del ENSP00000476242.2:n.-195-155del
ENST00000357590.9:c.-195-155del ENSP00000476176.2:n.-195-155del
ENST00000525039.5:n.229-155del
ENST00000525102.5:n.563-155del
ENST00000527992.5:n.33-155del
ENST00000530407.5:n.25-155del
ENST00000532085.1:n.1145del
ENST00000534384.1:n.26-155del
ENST00000538950.5:c.-344-155del ENSP00000475991.2:n.-344-155del
ENST00000545985.5:c.-195-155del ENSP00000475241.2:n.-195-155del
NM_001164277.1:c.-195-155del , LRG_187t1:c.-195-155del NP_001157749.1:n.-195-155del
NM_001164278.1:c.-195-155del NP_001157750.1:n.-195-155del
NM_001164279.1:c.-344-155del NP_001157751.1:n.-344-155del
NM_001467.5:c.-195-155del NP_001458.1:n.-195-155del
NM_001164278.2:c.-195-155del NP_001157750.1:n.-195-155del
NM_001164279.2:c.-344-155del NP_001157751.1:n.-344-155del
NM_001467.6:c.-195-155del NP_001458.1:n.-195-155del
NM_001164277.2:c.-195-155del MANE Select NP_001157749.1:n.-195-155del