Canonical Allele Identifier: CA2279174141

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1568063578

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727879A>G , CM000679.2:g.82727879A>G	GRCh38
NC_000017.10:g.80685755A>G , CM000679.1:g.80685755A>G	GRCh37
NC_000017.9:g.78279044A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*708A>G MANE Select	ENSP00000269373.6:n.*708A>G
ENST00000269373.10:c.*708A>G	ENSP00000269373.6:n.*708A>G
ENST00000571594.1:c.53+712A>G	ENSP00000459751.1:n.53+712A>G
NM_024619.3:c.*708A>G	NP_078895.2:n.*708A>G
NR_046408.1:n.1816A>G
XM_024450948.1:c.*708A>G	XP_024306716.1:n.*708A>G
NM_024619.4:c.*708A>G MANE Select	NP_078895.2:n.*708A>G
NR_046408.2:n.1816A>G