Canonical Allele Identifier: CA1474578055

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043277G= , CM000666.2:g.88043277G=	GRCh38
NC_000004.11:g.88964429G= , CM000666.1:g.88964429G=	GRCh37
NC_000004.10:g.89183453G=	NCBI36
NG_008604.1:g.40610G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1139G= MANE Select	ENSP00000237596.2:p.Trp380=
ENST00000237596.6:c.1139G=	ENSP00000237596.2:p.Trp380=
ENST00000506367.1:n.586G=
ENST00000508588.5:c.-379G=	ENSP00000427131.1:n.-379G=
NM_000297.3:c.1139G=	NP_000288.1:p.Trp380=
XM_011532028.1:c.1095-3365G=	XP_011530330.1:n.1095-3365G=
XM_011532029.1:c.419G=	XP_011530331.1:p.Trp140=
XM_011532030.1:c.299G=	XP_011530332.1:p.Trp100=
XR_244632.2:n.1234G=
NR_156488.1:n.1226G=
XM_011532028.2:c.1095-3365G=	XP_011530330.1:n.1095-3365G=
XM_011532030.2:c.299G=	XP_011530332.1:p.Trp100=
NM_000297.4:c.1139G= MANE Select	NP_000288.1:p.Trp380=
NR_156488.2:n.1238G=