Canonical Allele Identifier: CA1474579635

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046854A= , CM000666.2:g.88046854A=	GRCh38
NC_000004.11:g.88968006A= , CM000666.1:g.88968006A=	GRCh37
NC_000004.10:g.89187030A=	NCBI36
NG_008604.1:g.44187A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1532A= MANE Select	ENSP00000237596.2:p.Asp511=
ENST00000237596.6:c.1532A=	ENSP00000237596.2:p.Asp511=
ENST00000508588.5:c.-199+3397A=	ENSP00000427131.1:n.-199+3397A=
NM_000297.3:c.1532A=	NP_000288.1:p.Asp511=
XM_011532028.1:c.1307A=	XP_011530330.1:p.Asp436=
XM_011532029.1:c.812A=	XP_011530331.1:p.Asp271=
XM_011532030.1:c.692A=	XP_011530332.1:p.Asp231=
XR_244632.2:n.1627A=
NR_156488.1:n.1619A=
XM_011532028.2:c.1307A=	XP_011530330.1:p.Asp436=
XM_011532030.2:c.692A=	XP_011530332.1:p.Asp231=
NM_000297.4:c.1532A= MANE Select	NP_000288.1:p.Asp511=
NR_156488.2:n.1631A=