Canonical Allele Identifier: CA2103906

Gene: PNKD CATIP-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218339910C>T , CM000664.2:g.218339910C>T	GRCh38
NC_000002.11:g.219204633C>T , CM000664.1:g.219204633C>T	GRCh37
NC_000002.10:g.218912877C>T	NCBI36
NG_017060.1:g.74519C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015488.5:c.352+12C>T (PNKD) MANE Select	NP_056303.3:n.352+12C>T
ENST00000273077.9:c.352+12C>T (PNKD) MANE Select	ENSP00000273077.4:n.352+12C>T
NM_015488.4:c.352+12C>T (PNKD)	NP_056303.3:n.352+12C>T
NM_022572.4:c.280+12C>T (PNKD)	NP_072094.1:n.280+12C>T
NR_125777.1:n.120+11250G>A (CATIP-AS2)
ENST00000258362.7:c.280+12C>T (PNKD)	ENSP00000258362.3:n.280+12C>T
ENST00000273077.8:c.352+12C>T (PNKD)	ENSP00000273077.4:n.352+12C>T
ENST00000436005.2:c.172+12C>T (PNKD)	ENSP00000414400.2:n.172+12C>T
ENST00000436005.3:c.352+12C>T (PNKD)	ENSP00000414400.3:n.352+12C>T
ENST00000684905.1:n.363+12C>T (PNKD)
ENST00000685415.1:c.469+12C>T (PNKD)	ENSP00000510415.1:n.469+12C>T
ENST00000687736.1:c.352+12C>T (PNKD)	ENSP00000509627.1:n.352+12C>T
ENST00000688179.1:c.352+12C>T (PNKD)	ENSP00000508635.1:n.352+12C>T
ENST00000689098.1:n.269+12C>T (PNKD)
ENST00000689816.1:c.352+12C>T (PNKD)	ENSP00000508450.1:n.352+12C>T
ENST00000690891.1:c.497+12C>T (PNKD)	ENSP00000509744.1:n.497+12C>T
ENST00000691220.1:c.237-2071C>T (PNKD)	ENSP00000509580.1:n.237-2071C>T
ENST00000691799.1:n.240-4898C>T (PNKD)
ENST00000692295.1:c.165-1624C>T (PNKD)	ENSP00000509392.1:n.165-1624C>T
ENST00000693423.1:c.165-4545C>T (PNKD)	ENSP00000508705.1:n.165-4545C>T
XM_017003771.1:c.352+12C>T (PNKD)	XP_016859260.1:n.352+12C>T
XM_017003772.1:c.280+12C>T (PNKD)	XP_016859261.1:n.280+12C>T