Canonical Allele Identifier: CA2640699561

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727250-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727252del , CM000679.2:g.82727252del	GRCh38
NC_000017.10:g.80685128del , CM000679.1:g.80685128del	GRCh37
NC_000017.9:g.78278417del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*81del MANE Select	ENSP00000269373.6:n.*81del
ENST00000269373.10:c.*81del	ENSP00000269373.6:n.*81del
ENST00000571594.1:c.53+85del	ENSP00000459751.1:n.53+85del
ENST00000574832.5:c.*968del	ENSP00000460869.1:n.*968del
NM_024619.3:c.*81del	NP_078895.2:n.*81del
NR_046408.1:n.1189del
XM_024450948.1:c.*81del	XP_024306716.1:n.*81del
NM_024619.4:c.*81del MANE Select	NP_078895.2:n.*81del
NR_046408.2:n.1189del