Canonical Allele Identifier: CA986962020

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046846376
• gnomAD v3: 17-82727400-GGGATGTAT-G
• gnomAD v4: 17-82727400-GGGATGTAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727404_82727411del , CM000679.2:g.82727404_82727411del	GRCh38
NC_000017.10:g.80685280_80685287del , CM000679.1:g.80685280_80685287del	GRCh37
NC_000017.9:g.78278569_78278576del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*233_*240del MANE Select	ENSP00000269373.6:n.*233_*240del
ENST00000269373.10:c.*233_*240del	ENSP00000269373.6:n.*233_*240del
ENST00000571594.1:c.53+237_53+244del	ENSP00000459751.1:n.53+237_53+244del
ENST00000574832.5:c.*1120_*1127del	ENSP00000460869.1:n.*1120_*1127del
NM_024619.3:c.*233_*240del	NP_078895.2:n.*233_*240del
NR_046408.1:n.1341_1348del
XM_024450948.1:c.*233_*240del	XP_024306716.1:n.*233_*240del
NM_024619.4:c.*233_*240del MANE Select	NP_078895.2:n.*233_*240del
NR_046408.2:n.1341_1348del