Canonical Allele Identifier: CA2279173852

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046845534

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727273_82727274insAATAAGCAG , CM000679.2:g.82727273_82727274insAATAAGCAG	GRCh38
NC_000017.10:g.80685149_80685150insAATAAGCAG , CM000679.1:g.80685149_80685150insAATAAGCAG	GRCh37
NC_000017.9:g.78278438_78278439insAATAAGCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*102_*103insAATAAGCAG MANE Select	ENSP00000269373.6:n.*102_*103insAATAAGCAG
ENST00000269373.10:c.*102_*103insAATAAGCAG	ENSP00000269373.6:n.*102_*103insAATAAGCAG
ENST00000571594.1:c.53+106_53+107insAATAAGCAG	ENSP00000459751.1:n.53+106_53+107insAATAAGCAG
ENST00000574832.5:c.*989_*990insAATAAGCAG	ENSP00000460869.1:n.*989_*990insAATAAGCAG
NM_024619.3:c.*102_*103insAATAAGCAG	NP_078895.2:n.*102_*103insAATAAGCAG
NR_046408.1:n.1210_1211insAATAAGCAG
XM_024450948.1:c.*102_*103insAATAAGCAG	XP_024306716.1:n.*102_*103insAATAAGCAG
NM_024619.4:c.*102_*103insAATAAGCAG MANE Select	NP_078895.2:n.*102_*103insAATAAGCAG
NR_046408.2:n.1210_1211insAATAAGCAG