Canonical Allele Identifier: CA2663093559

Gene: PNKD

Linked Data

• gnomAD v4: 2-218270532-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218270532G>A , CM000664.2:g.218270532G>A	GRCh38
NC_000002.11:g.219135255G>A , CM000664.1:g.219135255G>A	GRCh37
NC_000002.10:g.218843499G>A	NCBI36
NG_017060.1:g.5141G>A
NG_033036.1:g.4639C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436005.3:c.-4G>A	ENSP00000414400.3:n.-4G>A
ENST00000472650.2:n.22G>A
ENST00000684905.1:n.8G>A
ENST00000685415.1:c.-4G>A	ENSP00000510415.1:n.-4G>A
ENST00000688179.1:c.-4G>A	ENSP00000508635.1:n.-4G>A
ENST00000689816.1:c.-4G>A	ENSP00000508450.1:n.-4G>A
ENST00000691799.1:n.70+812G>A
ENST00000692260.1:n.12G>A
ENST00000273077.9:c.-4G>A MANE Select	ENSP00000273077.4:n.-4G>A
ENST00000248451.7:c.-4G>A	ENSP00000248451.3:n.-4G>A
ENST00000273077.8:c.-4G>A	ENSP00000273077.4:n.-4G>A
ENST00000469689.1:n.13G>A
NM_001077399.2:c.-4G>A	NP_001070867.1:n.-4G>A
NM_015488.4:c.-4G>A	NP_056303.3:n.-4G>A
XM_017003771.1:c.-4G>A	XP_016859260.1:n.-4G>A
NM_015488.5:c.-4G>A MANE Select	NP_056303.3:n.-4G>A
NM_001077399.3:c.-4G>A	NP_001070867.1:n.-4G>A