Canonical Allele Identifier: CA2640698408

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727938-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727941_82727942dup , CM000679.2:g.82727941_82727942dup	GRCh38
NC_000017.10:g.80685817_80685818dup , CM000679.1:g.80685817_80685818dup	GRCh37
NC_000017.9:g.78279106_78279107dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*770_*771dup MANE Select	ENSP00000269373.6:n.*770_*771dup
ENST00000269373.10:c.*770_*771dup	ENSP00000269373.6:n.*770_*771dup
ENST00000571594.1:c.53+774_53+775dup	ENSP00000459751.1:n.53+774_53+775dup
NM_024619.3:c.*770_*771dup	NP_078895.2:n.*770_*771dup
NR_046408.1:n.1878_1879dup
XM_024450948.1:c.*770_*771dup	XP_024306716.1:n.*770_*771dup
NM_024619.4:c.*770_*771dup MANE Select	NP_078895.2:n.*770_*771dup
NR_046408.2:n.1878_1879dup