Canonical Allele Identifier: CA3096284132

Gene: PNKD

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218272739G= , CM000664.2:g.218272739G=	GRCh38
NC_000002.11:g.219137462G= , CM000664.1:g.219137462G=	GRCh37
NC_000002.10:g.218845706G=	NCBI36
NG_017060.1:g.7348G=
NG_033036.1:g.2432C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015488.5:c.236+1190G= MANE Select	NP_056303.3:n.236+1190G=
ENST00000273077.9:c.236+1190G= MANE Select	ENSP00000273077.4:n.236+1190G=
NM_001077399.2:c.406G=	NP_001070867.1:p.Val136=
NM_001077399.3:c.406G=	NP_001070867.1:p.Val136=
NM_015488.4:c.236+1190G=	NP_056303.3:n.236+1190G=
ENST00000248451.7:c.406G=	ENSP00000248451.3:p.Val136=
ENST00000273077.8:c.236+1190G=	ENSP00000273077.4:n.236+1190G=
ENST00000436005.3:c.236+1190G=	ENSP00000414400.3:n.236+1190G=
ENST00000469689.1:n.1200G=
ENST00000472650.1:n.170+1190G=
ENST00000472650.2:n.261+1190G=
ENST00000684905.1:n.247+1190G=
ENST00000685415.1:c.353+53G=	ENSP00000510415.1:n.353+53G=
ENST00000687736.1:c.236+1190G=	ENSP00000509627.1:n.236+1190G=
ENST00000688179.1:c.236+1190G=	ENSP00000508635.1:n.236+1190G=
ENST00000689816.1:c.236+1190G=	ENSP00000508450.1:n.236+1190G=
ENST00000690891.1:c.236+1190G=	ENSP00000509744.1:n.236+1190G=
ENST00000691220.1:c.236+1190G=	ENSP00000509580.1:n.236+1190G=
ENST00000691799.1:n.239+1190G=
ENST00000692260.1:n.1441G=
XM_017003771.1:c.236+1190G=	XP_016859260.1:n.236+1190G=