Canonical Allele Identifier: CA2616341202
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029891_119029892del , CM000673.2:g.119029891_119029892del GRCh38
NC_000011.9:g.118900601_118900602del , CM000673.1:g.118900601_118900602del GRCh37
NC_000011.8:g.118405811_118405812del NCBI36
NG_013331.1:g.6016_6017del , LRG_187:g.6016_6017del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-327_35-326del
ENST00000697846.1:n.35-327_35-326del
ENST00000697847.1:n.35-327_35-326del
ENST00000697848.1:n.35-327_35-326del
ENST00000697850.1:n.35-327_35-326del
ENST00000638186.1:n.84_85del
ENST00000638360.1:n.43-327_43-326del
ENST00000638925.1:n.42-327_42-326del
ENST00000650539.1:n.210+279_210+280del
ENST00000330775.9:c.-195-327_-195-326del ENSP00000476242.2:n.-195-327_-195-326del
ENST00000357590.9:c.-195-327_-195-326del ENSP00000476176.2:n.-195-327_-195-326del
ENST00000525039.5:n.229-327_229-326del
ENST00000525102.5:n.563-327_563-326del
ENST00000527992.5:n.33-327_33-326del
ENST00000530407.5:n.25-327_25-326del
ENST00000532085.1:n.973_974del
ENST00000534384.1:n.25+25_25+26del
ENST00000538950.5:c.-344-327_-344-326del ENSP00000475991.2:n.-344-327_-344-326del
ENST00000545985.5:c.-195-327_-195-326del ENSP00000475241.2:n.-195-327_-195-326del
NM_001164277.1:c.-195-327_-195-326del , LRG_187t1:c.-195-327_-195-326del NP_001157749.1:n.-195-327_-195-326del
NM_001164278.1:c.-195-327_-195-326del NP_001157750.1:n.-195-327_-195-326del
NM_001164279.1:c.-344-327_-344-326del NP_001157751.1:n.-344-327_-344-326del
NM_001467.5:c.-195-327_-195-326del NP_001458.1:n.-195-327_-195-326del
NM_001164278.2:c.-195-327_-195-326del NP_001157750.1:n.-195-327_-195-326del
NM_001164279.2:c.-344-327_-344-326del NP_001157751.1:n.-344-327_-344-326del
NM_001467.6:c.-195-327_-195-326del NP_001458.1:n.-195-327_-195-326del
NM_001164277.2:c.-195-327_-195-326del MANE Select NP_001157749.1:n.-195-327_-195-326del