Canonical Allele Identifier: CA1474579631

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046845A= , CM000666.2:g.88046845A=	GRCh38
NC_000004.11:g.88967997A= , CM000666.1:g.88967997A=	GRCh37
NC_000004.10:g.89187021A=	NCBI36
NG_008604.1:g.44178A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1523A= MANE Select	ENSP00000237596.2:p.Asn508=
ENST00000237596.6:c.1523A=	ENSP00000237596.2:p.Asn508=
ENST00000508588.5:c.-199+3388A=	ENSP00000427131.1:n.-199+3388A=
NM_000297.3:c.1523A=	NP_000288.1:p.Asn508=
XM_011532028.1:c.1298A=	XP_011530330.1:p.Asn433=
XM_011532029.1:c.803A=	XP_011530331.1:p.Asn268=
XM_011532030.1:c.683A=	XP_011530332.1:p.Asn228=
XR_244632.2:n.1618A=
NR_156488.1:n.1610A=
XM_011532028.2:c.1298A=	XP_011530330.1:p.Asn433=
XM_011532030.2:c.683A=	XP_011530332.1:p.Asn228=
NM_000297.4:c.1523A= MANE Select	NP_000288.1:p.Asn508=
NR_156488.2:n.1622A=