Canonical Allele Identifier: CA2810673897

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727666_82727667insCG , CM000679.2:g.82727666_82727667insCG	GRCh38
NC_000017.10:g.80685542_80685543insCG , CM000679.1:g.80685542_80685543insCG	GRCh37
NC_000017.9:g.78278831_78278832insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*495_*496insCG MANE Select	ENSP00000269373.6:n.*495_*496insCG
ENST00000269373.10:c.*495_*496insCG	ENSP00000269373.6:n.*495_*496insCG
ENST00000571594.1:c.53+499_53+500insCG	ENSP00000459751.1:n.53+499_53+500insCG
NM_024619.3:c.*495_*496insCG	NP_078895.2:n.*495_*496insCG
NR_046408.1:n.1603_1604insCG
XM_024450948.1:c.*495_*496insCG	XP_024306716.1:n.*495_*496insCG
NM_024619.4:c.*495_*496insCG MANE Select	NP_078895.2:n.*495_*496insCG
NR_046408.2:n.1603_1604insCG