Canonical Allele Identifier: CA656898286

Gene: FN3KRP

Linked Data

• COSMIC: COSN19411583

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727236_82727237insA , CM000679.2:g.82727236_82727237insA	GRCh38
NC_000017.10:g.80685112_80685113insA , CM000679.1:g.80685112_80685113insA	GRCh37
NC_000017.9:g.78278401_78278402insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*65_*66insA MANE Select	ENSP00000269373.6:n.*65_*66insA
ENST00000269373.10:c.*65_*66insA	ENSP00000269373.6:n.*65_*66insA
ENST00000571594.1:c.53+69_53+70insA	ENSP00000459751.1:n.53+69_53+70insA
ENST00000574832.5:c.*952_*953insA	ENSP00000460869.1:n.*952_*953insA
NM_024619.3:c.*65_*66insA	NP_078895.2:n.*65_*66insA
NR_046408.1:n.1173_1174insA
XM_024450948.1:c.*65_*66insA	XP_024306716.1:n.*65_*66insA
NM_024619.4:c.*65_*66insA MANE Select	NP_078895.2:n.*65_*66insA
NR_046408.2:n.1173_1174insA