Canonical Allele Identifier: CA1474575796

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038280G= , CM000666.2:g.88038280G=	GRCh38
NC_000004.11:g.88959432G= , CM000666.1:g.88959432G=	GRCh37
NC_000004.10:g.89178456G=	NCBI36
NG_008604.1:g.35613G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237596.7:c.873G= MANE Select	ENSP00000237596.2:p.Leu291=
ENST00000237596.6:c.873G=	ENSP00000237596.2:p.Leu291=
ENST00000506367.1:n.320G=
ENST00000506727.1:n.459G=
NM_000297.3:c.873G=	NP_000288.1:p.Leu291=
XM_011532028.1:c.873G=	XP_011530330.1:p.Leu291=
XM_011532029.1:c.153G=	XP_011530331.1:p.Leu51=
XM_011532030.1:c.33G=	XP_011530332.1:p.Leu11=
XR_244632.2:n.968G=
NR_156488.1:n.960G=
XM_011532028.2:c.873G=	XP_011530330.1:p.Leu291=
XM_011532030.2:c.33G=	XP_011530332.1:p.Leu11=
NM_000297.4:c.873G= MANE Select	NP_000288.1:p.Leu291=
NR_156488.2:n.972G=