Canonical Allele Identifier: CA1474579669

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046911C= , CM000666.2:g.88046911C=	GRCh38
NC_000004.11:g.88968063C= , CM000666.1:g.88968063C=	GRCh37
NC_000004.10:g.89187087C=	NCBI36
NG_008604.1:g.44244C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+41C= MANE Select	ENSP00000237596.2:n.1548+41C=
ENST00000237596.6:c.1548+41C=	ENSP00000237596.2:n.1548+41C=
ENST00000508588.5:c.-199+3454C=	ENSP00000427131.1:n.-199+3454C=
NM_000297.3:c.1548+41C=	NP_000288.1:n.1548+41C=
XM_011532028.1:c.1323+41C=	XP_011530330.1:n.1323+41C=
XM_011532029.1:c.828+41C=	XP_011530331.1:n.828+41C=
XM_011532030.1:c.708+41C=	XP_011530332.1:n.708+41C=
XR_244632.2:n.1643+41C=
NR_156488.1:n.1635+41C=
XM_011532028.2:c.1323+41C=	XP_011530330.1:n.1323+41C=
XM_011532030.2:c.708+41C=	XP_011530332.1:n.708+41C=
NM_000297.4:c.1548+41C= MANE Select	NP_000288.1:n.1548+41C=
NR_156488.2:n.1647+41C=