Canonical Allele Identifier: CA986962246

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046850843
• gnomAD v3: 17-82727970-TC-T
• gnomAD v4: 17-82727970-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727972del , CM000679.2:g.82727972del	GRCh38
NC_000017.10:g.80685848del , CM000679.1:g.80685848del	GRCh37
NC_000017.9:g.78279137del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*801del MANE Select	ENSP00000269373.6:n.*801del
ENST00000269373.10:c.*801del	ENSP00000269373.6:n.*801del
ENST00000571594.1:c.53+805del	ENSP00000459751.1:n.53+805del
NM_024619.3:c.*801del	NP_078895.2:n.*801del
NR_046408.1:n.1909del
XM_024450948.1:c.*801del	XP_024306716.1:n.*801del
NM_024619.4:c.*801del MANE Select	NP_078895.2:n.*801del
NR_046408.2:n.1909del