Canonical Allele Identifier: CA2279173920

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046846591

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727433_82727435del , CM000679.2:g.82727433_82727435del	GRCh38
NC_000017.10:g.80685309_80685311del , CM000679.1:g.80685309_80685311del	GRCh37
NC_000017.9:g.78278598_78278600del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*262_*264del MANE Select	ENSP00000269373.6:n.*262_*264del
ENST00000269373.10:c.*262_*264del	ENSP00000269373.6:n.*262_*264del
ENST00000571594.1:c.53+266_53+268del	ENSP00000459751.1:n.53+266_53+268del
ENST00000574832.5:c.*1149_*1151del	ENSP00000460869.1:n.*1149_*1151del
NM_024619.3:c.*262_*264del	NP_078895.2:n.*262_*264del
NR_046408.1:n.1370_1372del
XM_024450948.1:c.*262_*264del	XP_024306716.1:n.*262_*264del
NM_024619.4:c.*262_*264del MANE Select	NP_078895.2:n.*262_*264del
NR_046408.2:n.1370_1372del