Canonical Allele Identifier: CA2344950083
Gene: SLC27A5 HGNC NCBI
ZNF446 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.58488006A= , CM000681.2:g.58488006A= GRCh38
NC_000019.9:g.58999373A= , CM000681.1:g.58999373A= GRCh37
NC_000019.8:g.63691185A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000595851.5:c.*22-4360T= (SLC27A5) ENSP00000469512.1:n.*22-4360T=
NM_001304453.1:c.803-1284A= (ZNF446) NP_001291382.1:n.803-1284A=
XM_006723266.2:c.803-1284A= (ZNF446) XP_006723329.1:n.803-1284A=
XM_006723266.4:c.803-1284A= (ZNF446) XP_006723329.1:n.803-1284A=
XM_017026950.2:c.1005-1284A= (ZNF446) XP_016882439.1:n.1005-1284A=
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