Canonical Allele Identifier: CA2616341137
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029798_119029804del , CM000673.2:g.119029798_119029804del GRCh38
NC_000011.9:g.118900508_118900514del , CM000673.1:g.118900508_118900514del GRCh37
NC_000011.8:g.118405718_118405724del NCBI36
NG_013331.1:g.6104_6110del , LRG_187:g.6104_6110del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-239_35-233del
ENST00000697846.1:n.35-239_35-233del
ENST00000697847.1:n.35-239_35-233del
ENST00000697848.1:n.35-239_35-233del
ENST00000697849.1:n.40_46del
ENST00000697850.1:n.35-239_35-233del
ENST00000697851.1:n.40_46del
ENST00000638186.1:n.108+64_108+70del
ENST00000638360.1:n.43-239_43-233del
ENST00000638925.1:n.42-239_42-233del
ENST00000650539.1:n.211-239_211-233del
ENST00000330775.9:c.-195-239_-195-233del ENSP00000476242.2:n.-195-239_-195-233del
ENST00000357590.9:c.-195-239_-195-233del ENSP00000476176.2:n.-195-239_-195-233del
ENST00000525039.5:n.229-239_229-233del
ENST00000525102.5:n.563-239_563-233del
ENST00000527992.5:n.33-239_33-233del
ENST00000530407.5:n.25-239_25-233del
ENST00000532085.1:n.1061_1067del
ENST00000534384.1:n.25+113_25+119del
ENST00000538950.5:c.-344-239_-344-233del ENSP00000475991.2:n.-344-239_-344-233del
ENST00000545985.5:c.-195-239_-195-233del ENSP00000475241.2:n.-195-239_-195-233del
NM_001164277.1:c.-195-239_-195-233del , LRG_187t1:c.-195-239_-195-233del NP_001157749.1:n.-195-239_-195-233del
NM_001164278.1:c.-195-239_-195-233del NP_001157750.1:n.-195-239_-195-233del
NM_001164279.1:c.-344-239_-344-233del NP_001157751.1:n.-344-239_-344-233del
NM_001467.5:c.-195-239_-195-233del NP_001458.1:n.-195-239_-195-233del
NM_001164278.2:c.-195-239_-195-233del NP_001157750.1:n.-195-239_-195-233del
NM_001164279.2:c.-344-239_-344-233del NP_001157751.1:n.-344-239_-344-233del
NM_001467.6:c.-195-239_-195-233del NP_001458.1:n.-195-239_-195-233del
NM_001164277.2:c.-195-239_-195-233del MANE Select NP_001157749.1:n.-195-239_-195-233del