Canonical Allele Identifier: CA2640699616

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727277-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727279del , CM000679.2:g.82727279del	GRCh38
NC_000017.10:g.80685155del , CM000679.1:g.80685155del	GRCh37
NC_000017.9:g.78278444del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*108del MANE Select	ENSP00000269373.6:n.*108del
ENST00000269373.10:c.*108del	ENSP00000269373.6:n.*108del
ENST00000571594.1:c.53+112del	ENSP00000459751.1:n.53+112del
ENST00000574832.5:c.*995del	ENSP00000460869.1:n.*995del
NM_024619.3:c.*108del	NP_078895.2:n.*108del
NR_046408.1:n.1216del
XM_024450948.1:c.*108del	XP_024306716.1:n.*108del
NM_024619.4:c.*108del MANE Select	NP_078895.2:n.*108del
NR_046408.2:n.1216del