Canonical Allele Identifier: CA2663093795

Gene: PNKD

Linked Data

• gnomAD v4: 2-218270619-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218270619_218270620insT , CM000664.2:g.218270619_218270620insT	GRCh38
NC_000002.11:g.219135342_219135343insT , CM000664.1:g.219135342_219135343insT	GRCh37
NC_000002.10:g.218843586_218843587insT	NCBI36
NG_017060.1:g.5228_5229insT
NG_033036.1:g.4551_4552insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436005.3:c.67+17_67+18insT	ENSP00000414400.3:n.67+17_67+18insT
ENST00000472650.2:n.92+17_92+18insT
ENST00000684905.1:n.78+17_78+18insT
ENST00000685415.1:c.67+17_67+18insT	ENSP00000510415.1:n.67+17_67+18insT
ENST00000687736.1:c.67+17_67+18insT	ENSP00000509627.1:n.67+17_67+18insT
ENST00000688179.1:c.67+17_67+18insT	ENSP00000508635.1:n.67+17_67+18insT
ENST00000689816.1:c.67+17_67+18insT	ENSP00000508450.1:n.67+17_67+18insT
ENST00000690891.1:c.67+17_67+18insT	ENSP00000509744.1:n.67+17_67+18insT
ENST00000691220.1:c.67+17_67+18insT	ENSP00000509580.1:n.67+17_67+18insT
ENST00000691799.1:n.71-762_71-761insT
ENST00000692260.1:n.82+17_82+18insT
ENST00000273077.9:c.67+17_67+18insT MANE Select	ENSP00000273077.4:n.67+17_67+18insT
ENST00000248451.7:c.67+17_67+18insT	ENSP00000248451.3:n.67+17_67+18insT
ENST00000273077.8:c.67+17_67+18insT	ENSP00000273077.4:n.67+17_67+18insT
ENST00000469689.1:n.100_101insT
NM_001077399.2:c.67+17_67+18insT	NP_001070867.1:n.67+17_67+18insT
NM_015488.4:c.67+17_67+18insT	NP_056303.3:n.67+17_67+18insT
XM_017003771.1:c.67+17_67+18insT	XP_016859260.1:n.67+17_67+18insT
NM_015488.5:c.67+17_67+18insT MANE Select	NP_056303.3:n.67+17_67+18insT
NM_001077399.3:c.67+17_67+18insT	NP_001070867.1:n.67+17_67+18insT