Canonical Allele Identifier: CA431226371

Gene: PNKD

Linked Data

• MyVariant Identifiers: chr2:g.219135304A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218270581A>C , CM000664.2:g.218270581A>C	GRCh38
NC_000002.11:g.219135304A>C , CM000664.1:g.219135304A>C	GRCh37
NC_000002.10:g.218843548A>C	NCBI36
NG_017060.1:g.5190A>C
NG_033036.1:g.4590T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436005.3:c.46A>C	ENSP00000414400.3:p.Arg16=
ENST00000472650.2:n.71A>C
ENST00000684905.1:n.57A>C
ENST00000685415.1:c.46A>C	ENSP00000510415.1:p.Arg16=
ENST00000687736.1:c.46A>C	ENSP00000509627.1:p.Arg16=
ENST00000688179.1:c.46A>C	ENSP00000508635.1:p.Arg16=
ENST00000689816.1:c.46A>C	ENSP00000508450.1:p.Arg16=
ENST00000690891.1:c.46A>C	ENSP00000509744.1:p.Arg16=
ENST00000691220.1:c.46A>C	ENSP00000509580.1:p.Arg16=
ENST00000691799.1:n.71-800A>C
ENST00000692260.1:n.61A>C
ENST00000273077.9:c.46A>C MANE Select	ENSP00000273077.4:p.Arg16=
ENST00000248451.7:c.46A>C	ENSP00000248451.3:p.Arg16=
ENST00000273077.8:c.46A>C	ENSP00000273077.4:p.Arg16=
ENST00000469689.1:n.62A>C
NM_001077399.2:c.46A>C	NP_001070867.1:p.Arg16=
NM_015488.4:c.46A>C	NP_056303.3:p.Arg16=
XM_017003771.1:c.46A>C	XP_016859260.1:p.Arg16=
NM_015488.5:c.46A>C MANE Select	NP_056303.3:p.Arg16=
NM_001077399.3:c.46A>C	NP_001070867.1:p.Arg16=