Canonical Allele Identifier: CA1474578087

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043346C= , CM000666.2:g.88043346C=	GRCh38
NC_000004.11:g.88964498C= , CM000666.1:g.88964498C=	GRCh37
NC_000004.10:g.89183522C=	NCBI36
NG_008604.1:g.40679C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1208C= MANE Select	ENSP00000237596.2:p.Ala403=
ENST00000237596.6:c.1208C=	ENSP00000237596.2:p.Ala403=
ENST00000506367.1:n.655C=
ENST00000508588.5:c.-310C=	ENSP00000427131.1:n.-310C=
NM_000297.3:c.1208C=	NP_000288.1:p.Ala403=
XM_011532028.1:c.1095-3296C=	XP_011530330.1:n.1095-3296C=
XM_011532029.1:c.488C=	XP_011530331.1:p.Ala163=
XM_011532030.1:c.368C=	XP_011530332.1:p.Ala123=
XR_244632.2:n.1303C=
NR_156488.1:n.1295C=
XM_011532028.2:c.1095-3296C=	XP_011530330.1:n.1095-3296C=
XM_011532030.2:c.368C=	XP_011530332.1:p.Ala123=
NM_000297.4:c.1208C= MANE Select	NP_000288.1:p.Ala403=
NR_156488.2:n.1307C=