Canonical Allele Identifier: CA2616340746
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029496del , CM000673.2:g.119029496del GRCh38
NC_000011.9:g.118900206del , CM000673.1:g.118900206del GRCh37
NC_000011.8:g.118405416del NCBI36
NG_013331.1:g.6413del , LRG_187:g.6413del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.105del
ENST00000697846.1:n.105del
ENST00000697847.1:n.105del
ENST00000697848.1:n.105del
ENST00000697849.1:n.349del
ENST00000697850.1:n.105del
ENST00000697851.1:n.349del
ENST00000638186.1:n.179del
ENST00000638360.1:n.113del
ENST00000638925.1:n.112del
ENST00000650539.1:n.281del
ENST00000330775.9:c.-125del ENSP00000476242.2:n.-125del
ENST00000357590.9:c.-125del ENSP00000476176.2:n.-125del
ENST00000525039.5:n.299del
ENST00000525102.5:n.633del
ENST00000525787.1:n.171del
ENST00000526626.6:n.71del
ENST00000527992.5:n.103del
ENST00000530407.5:n.95del
ENST00000532085.1:n.1370del
ENST00000532888.6:n.71del
ENST00000534384.1:n.96del
ENST00000538950.5:c.-274del ENSP00000475991.2:n.-274del
ENST00000545985.5:c.-125del ENSP00000475241.2:n.-125del
NM_001164277.1:c.-125del , LRG_187t1:c.-125del NP_001157749.1:n.-125del
NM_001164278.1:c.-125del NP_001157750.1:n.-125del
NM_001164279.1:c.-274del NP_001157751.1:n.-274del
NM_001164280.1:c.-125del NP_001157752.1:n.-125del
NM_001467.5:c.-125del NP_001458.1:n.-125del
NM_001164278.2:c.-125del NP_001157750.1:n.-125del
NM_001164279.2:c.-274del NP_001157751.1:n.-274del
NM_001467.6:c.-125del NP_001458.1:n.-125del
NM_001164277.2:c.-125del MANE Select NP_001157749.1:n.-125del