Canonical Allele Identifier: CA440263322

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967962C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046810C>T , CM000666.2:g.88046810C>T	GRCh38
NC_000004.11:g.88967962C>T , CM000666.1:g.88967962C>T	GRCh37
NC_000004.10:g.89186986C>T	NCBI36
NG_008604.1:g.44143C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1488C>T MANE Select	ENSP00000237596.2:p.Arg496=
ENST00000237596.6:c.1488C>T	ENSP00000237596.2:p.Arg496=
ENST00000508588.5:c.-199+3353C>T	ENSP00000427131.1:n.-199+3353C>T
NM_000297.3:c.1488C>T	NP_000288.1:p.Arg496=
XM_011532028.1:c.1263C>T	XP_011530330.1:p.Arg421=
XM_011532029.1:c.768C>T	XP_011530331.1:p.Arg256=
XM_011532030.1:c.648C>T	XP_011530332.1:p.Arg216=
XR_244632.2:n.1583C>T
NR_156488.1:n.1575C>T
XM_011532028.2:c.1263C>T	XP_011530330.1:p.Arg421=
XM_011532030.2:c.648C>T	XP_011530332.1:p.Arg216=
NM_000297.4:c.1488C>T MANE Select	NP_000288.1:p.Arg496=
NR_156488.2:n.1587C>T