Canonical Allele Identifier: CA884062179

Gene: SLC27A5 ZNF446

Linked Data

• dbSNP Id: rs1194007545
• gnomAD v3: 19-58487903-A-G
• gnomAD v4: 19-58487903-A-G
• MyVariant Identifiers: chr19:g.58999270A>G (hg19) ; chr19:g.58487903A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.58487903A>G , CM000681.2:g.58487903A>G	GRCh38
NC_000019.9:g.58999270A>G , CM000681.1:g.58999270A>G	GRCh37
NC_000019.8:g.63691082A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000595851.5:c.*22-4257T>C (SLC27A5)	ENSP00000469512.1:n.*22-4257T>C
NM_001304453.1:c.803-1387A>G (ZNF446)	NP_001291382.1:n.803-1387A>G
XM_006723266.2:c.803-1387A>G (ZNF446)	XP_006723329.1:n.803-1387A>G
XM_006723266.4:c.803-1387A>G (ZNF446)	XP_006723329.1:n.803-1387A>G
XM_017026950.2:c.1005-1387A>G (ZNF446)	XP_016882439.1:n.1005-1387A>G