Canonical Allele Identifier: CA1474579720

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88047026A= , CM000666.2:g.88047026A=	GRCh38
NC_000004.11:g.88968178A= , CM000666.1:g.88968178A=	GRCh37
NC_000004.10:g.89187202A=	NCBI36
NG_008604.1:g.44359A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1548+156A= MANE Select	ENSP00000237596.2:n.1548+156A=
ENST00000237596.6:c.1548+156A=	ENSP00000237596.2:n.1548+156A=
ENST00000508588.5:c.-199+3569A=	ENSP00000427131.1:n.-199+3569A=
NM_000297.3:c.1548+156A=	NP_000288.1:n.1548+156A=
XM_011532028.1:c.1323+156A=	XP_011530330.1:n.1323+156A=
XM_011532029.1:c.828+156A=	XP_011530331.1:n.828+156A=
XM_011532030.1:c.708+156A=	XP_011530332.1:n.708+156A=
XR_244632.2:n.1643+156A=
NR_156488.1:n.1635+156A=
XM_011532028.2:c.1323+156A=	XP_011530330.1:n.1323+156A=
XM_011532030.2:c.708+156A=	XP_011530332.1:n.708+156A=
NM_000297.4:c.1548+156A= MANE Select	NP_000288.1:n.1548+156A=
NR_156488.2:n.1647+156A=