Canonical Allele Identifier: CA2640697216

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727339-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727339_82727340insA , CM000679.2:g.82727339_82727340insA	GRCh38
NC_000017.10:g.80685215_80685216insA , CM000679.1:g.80685215_80685216insA	GRCh37
NC_000017.9:g.78278504_78278505insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*168_*169insA MANE Select	ENSP00000269373.6:n.*168_*169insA
ENST00000269373.10:c.*168_*169insA	ENSP00000269373.6:n.*168_*169insA
ENST00000571594.1:c.53+172_53+173insA	ENSP00000459751.1:n.53+172_53+173insA
ENST00000574832.5:c.*1055_*1056insA	ENSP00000460869.1:n.*1055_*1056insA
NM_024619.3:c.*168_*169insA	NP_078895.2:n.*168_*169insA
NR_046408.1:n.1276_1277insA
XM_024450948.1:c.*168_*169insA	XP_024306716.1:n.*168_*169insA
NM_024619.4:c.*168_*169insA MANE Select	NP_078895.2:n.*168_*169insA
NR_046408.2:n.1276_1277insA