Canonical Allele Identifier: CA2640697202

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727330-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727333del , CM000679.2:g.82727333del	GRCh38
NC_000017.10:g.80685209del , CM000679.1:g.80685209del	GRCh37
NC_000017.9:g.78278498del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*162del MANE Select	ENSP00000269373.6:n.*162del
ENST00000269373.10:c.*162del	ENSP00000269373.6:n.*162del
ENST00000571594.1:c.53+166del	ENSP00000459751.1:n.53+166del
ENST00000574832.5:c.*1049del	ENSP00000460869.1:n.*1049del
NM_024619.3:c.*162del	NP_078895.2:n.*162del
NR_046408.1:n.1270del
XM_024450948.1:c.*162del	XP_024306716.1:n.*162del
NM_024619.4:c.*162del MANE Select	NP_078895.2:n.*162del
NR_046408.2:n.1270del