Canonical Allele Identifier: CA65763063

Gene: PNKD CATIP-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218346471G>A , CM000664.2:g.218346471G>A	GRCh38
NC_000002.11:g.219211194G>A , CM000664.1:g.219211194G>A	GRCh37
NC_000002.10:g.218919438G>A	NCBI36
NG_017060.1:g.81080G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015488.5:c.*1490G>A (PNKD) MANE Select	NP_056303.3:n.*1490G>A
ENST00000273077.9:c.*1490G>A (PNKD) MANE Select	ENSP00000273077.4:n.*1490G>A
NM_015488.4:c.*1490G>A (PNKD)	NP_056303.3:n.*1490G>A
NM_022572.4:c.*1490G>A (PNKD)	NP_072094.1:n.*1490G>A
NR_125777.1:n.120+4689C>T (CATIP-AS2)
ENST00000258362.7:c.*1490G>A (PNKD)	ENSP00000258362.3:n.*1490G>A
ENST00000273077.8:c.*1490G>A (PNKD)	ENSP00000273077.4:n.*1490G>A
ENST00000436005.3:c.*1490G>A (PNKD)	ENSP00000414400.3:n.*1490G>A
ENST00000684905.1:n.3406G>A (PNKD)
ENST00000685415.1:c.*1490G>A (PNKD)	ENSP00000510415.1:n.*1490G>A
ENST00000687736.1:c.2468G>A (PNKD)	ENSP00000509627.1:n.2468G>A
ENST00000688179.1:c.*1490G>A (PNKD)	ENSP00000508635.1:n.*1490G>A
ENST00000689098.1:n.3312G>A (PNKD)
ENST00000689693.1:n.3445G>A (PNKD)
ENST00000689816.1:c.*1490G>A (PNKD)	ENSP00000508450.1:n.*1490G>A
ENST00000690891.1:c.2793G>A (PNKD)	ENSP00000509744.1:n.2793G>A
ENST00000691220.1:c.2267G>A (PNKD)	ENSP00000509580.1:n.2267G>A
ENST00000691799.1:n.1903G>A (PNKD)
ENST00000692295.1:c.2288G>A (PNKD)	ENSP00000509392.1:n.2288G>A
ENST00000693423.1:c.*1773G>A (PNKD)	ENSP00000508705.1:n.*1773G>A
ENST00000693556.1:n.1970G>A (PNKD)
XM_017003771.1:c.*1490G>A (PNKD)	XP_016859260.1:n.*1490G>A
XM_017003772.1:c.*1490G>A (PNKD)	XP_016859261.1:n.*1490G>A