Canonical Allele Identifier: CA1474578077

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043324T= , CM000666.2:g.88043324T=	GRCh38
NC_000004.11:g.88964476T= , CM000666.1:g.88964476T=	GRCh37
NC_000004.10:g.89183500T=	NCBI36
NG_008604.1:g.40657T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1186T= MANE Select	ENSP00000237596.2:p.Ser396=
ENST00000237596.6:c.1186T=	ENSP00000237596.2:p.Ser396=
ENST00000506367.1:n.633T=
ENST00000508588.5:c.-332T=	ENSP00000427131.1:n.-332T=
NM_000297.3:c.1186T=	NP_000288.1:p.Ser396=
XM_011532028.1:c.1095-3318T=	XP_011530330.1:n.1095-3318T=
XM_011532029.1:c.466T=	XP_011530331.1:p.Ser156=
XM_011532030.1:c.346T=	XP_011530332.1:p.Ser116=
XR_244632.2:n.1281T=
NR_156488.1:n.1273T=
XM_011532028.2:c.1095-3318T=	XP_011530330.1:n.1095-3318T=
XM_011532030.2:c.346T=	XP_011530332.1:p.Ser116=
NM_000297.4:c.1186T= MANE Select	NP_000288.1:p.Ser396=
NR_156488.2:n.1285T=