Canonical Allele Identifier: CA775764061

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1299306473
• MyVariant Identifiers: chr17:g.80685116C>T (hg19) ; chr17:g.82727240C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727240C>T , CM000679.2:g.82727240C>T	GRCh38
NC_000017.10:g.80685116C>T , CM000679.1:g.80685116C>T	GRCh37
NC_000017.9:g.78278405C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*69C>T MANE Select	ENSP00000269373.6:n.*69C>T
ENST00000269373.10:c.*69C>T	ENSP00000269373.6:n.*69C>T
ENST00000571594.1:c.53+73C>T	ENSP00000459751.1:n.53+73C>T
ENST00000574832.5:c.*956C>T	ENSP00000460869.1:n.*956C>T
NM_024619.3:c.*69C>T	NP_078895.2:n.*69C>T
NR_046408.1:n.1177C>T
XM_024450948.1:c.*69C>T	XP_024306716.1:n.*69C>T
NM_024619.4:c.*69C>T MANE Select	NP_078895.2:n.*69C>T
NR_046408.2:n.1177C>T