Canonical Allele Identifier: CA997545986

Gene: SLC27A5 ZNF446

Linked Data

• dbSNP Id: rs2053177855
• gnomAD v3: 19-58488003-C-CCCG
• gnomAD v4: 19-58488003-C-CCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.58488003_58488004insCCG , CM000681.2:g.58488003_58488004insCCG	GRCh38
NC_000019.9:g.58999370_58999371insCCG , CM000681.1:g.58999370_58999371insCCG	GRCh37
NC_000019.8:g.63691182_63691183insCCG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000595851.5:c.*22-4358_*22-4357insCGG (SLC27A5)	ENSP00000469512.1:n.*22-4358_*22-4357insC...
NM_001304453.1:c.803-1287_803-1286insCCG (ZNF446)	NP_001291382.1:n.803-1287_803-1286insCCG
XM_006723266.2:c.803-1287_803-1286insCCG (ZNF446)	XP_006723329.1:n.803-1287_803-1286insCCG
XM_006723266.4:c.803-1287_803-1286insCCG (ZNF446)	XP_006723329.1:n.803-1287_803-1286insCCG
XM_017026950.2:c.1005-1287_1005-1286insCCG (ZNF446)	XP_016882439.1:n.1005-1287_1005-1286insCC...