Canonical Allele Identifier: CA2279173901

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046846299

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727394_82727405del , CM000679.2:g.82727394_82727405del	GRCh38
NC_000017.10:g.80685270_80685281del , CM000679.1:g.80685270_80685281del	GRCh37
NC_000017.9:g.78278559_78278570del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*223_*234del MANE Select	ENSP00000269373.6:n.*223_*234del
ENST00000269373.10:c.*223_*234del	ENSP00000269373.6:n.*223_*234del
ENST00000571594.1:c.53+227_53+238del	ENSP00000459751.1:n.53+227_53+238del
ENST00000574832.5:c.*1110_*1121del	ENSP00000460869.1:n.*1110_*1121del
NM_024619.3:c.*223_*234del	NP_078895.2:n.*223_*234del
NR_046408.1:n.1331_1342del
XM_024450948.1:c.*223_*234del	XP_024306716.1:n.*223_*234del
NM_024619.4:c.*223_*234del MANE Select	NP_078895.2:n.*223_*234del
NR_046408.2:n.1331_1342del