Canonical Allele Identifier: CA2640699518

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727222-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727222_82727223insCTG , CM000679.2:g.82727222_82727223insCTG	GRCh38
NC_000017.10:g.80685098_80685099insCTG , CM000679.1:g.80685098_80685099insCTG	GRCh37
NC_000017.9:g.78278387_78278388insCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*51_*52insCTG MANE Select	ENSP00000269373.6:n.*51_*52insCTG
ENST00000269373.10:c.*51_*52insCTG	ENSP00000269373.6:n.*51_*52insCTG
ENST00000571594.1:c.53+55_53+56insCTG	ENSP00000459751.1:n.53+55_53+56insCTG
ENST00000574832.5:c.*938_*939insCTG	ENSP00000460869.1:n.*938_*939insCTG
NM_024619.3:c.*51_*52insCTG	NP_078895.2:n.*51_*52insCTG
NR_046408.1:n.1159_1160insCTG
XM_024450948.1:c.*51_*52insCTG	XP_024306716.1:n.*51_*52insCTG
NM_024619.4:c.*51_*52insCTG MANE Select	NP_078895.2:n.*51_*52insCTG
NR_046408.2:n.1159_1160insCTG