Canonical Allele Identifier: CA2279174193

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046850824

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727970del , CM000679.2:g.82727970del	GRCh38
NC_000017.10:g.80685846del , CM000679.1:g.80685846del	GRCh37
NC_000017.9:g.78279135del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*799del MANE Select	ENSP00000269373.6:n.*799del
ENST00000269373.10:c.*799del	ENSP00000269373.6:n.*799del
ENST00000571594.1:c.53+803del	ENSP00000459751.1:n.53+803del
NM_024619.3:c.*799del	NP_078895.2:n.*799del
NR_046408.1:n.1907del
XM_024450948.1:c.*799del	XP_024306716.1:n.*799del
NM_024619.4:c.*799del MANE Select	NP_078895.2:n.*799del
NR_046408.2:n.1907del