Canonical Allele Identifier: CA1474579601

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046781T= , CM000666.2:g.88046781T=	GRCh38
NC_000004.11:g.88967933T= , CM000666.1:g.88967933T=	GRCh37
NC_000004.10:g.89186957T=	NCBI36
NG_008604.1:g.44114T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1459T= MANE Select	ENSP00000237596.2:p.Tyr487=
ENST00000237596.6:c.1459T=	ENSP00000237596.2:p.Tyr487=
ENST00000508588.5:c.-199+3324T=	ENSP00000427131.1:n.-199+3324T=
NM_000297.3:c.1459T=	NP_000288.1:p.Tyr487=
XM_011532028.1:c.1234T=	XP_011530330.1:p.Tyr412=
XM_011532029.1:c.739T=	XP_011530331.1:p.Tyr247=
XM_011532030.1:c.619T=	XP_011530332.1:p.Tyr207=
XR_244632.2:n.1554T=
NR_156488.1:n.1546T=
XM_011532028.2:c.1234T=	XP_011530330.1:p.Tyr412=
XM_011532030.2:c.619T=	XP_011530332.1:p.Tyr207=
NM_000297.4:c.1459T= MANE Select	NP_000288.1:p.Tyr487=
NR_156488.2:n.1558T=