Canonical Allele Identifier: CA357615422

Gene: PKD2

Linked Data

• dbSNP Id: rs1727643488
• MyVariant Identifiers: chr4:g.88964402A>C (hg19) ; chr4:g.88043250A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88043250A>C , CM000666.2:g.88043250A>C	GRCh38
NC_000004.11:g.88964402A>C , CM000666.1:g.88964402A>C	GRCh37
NC_000004.10:g.89183426A>C	NCBI36
NG_008604.1:g.40583A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1112A>C MANE Select	ENSP00000237596.2:p.Glu371Ala
ENST00000237596.6:c.1112A>C	ENSP00000237596.2:p.Glu371Ala
ENST00000506367.1:n.559A>C
NM_000297.3:c.1112A>C	NP_000288.1:p.Glu371Ala
XM_011532028.1:c.1095-3392A>C	XP_011530330.1:n.1095-3392A>C
XM_011532029.1:c.392A>C	XP_011530331.1:p.Glu131Ala
XM_011532030.1:c.272A>C	XP_011530332.1:p.Glu91Ala
XR_244632.2:n.1207A>C
NR_156488.1:n.1199A>C
XM_011532028.2:c.1095-3392A>C	XP_011530330.1:n.1095-3392A>C
XM_011532030.2:c.272A>C	XP_011530332.1:p.Glu91Ala
NM_000297.4:c.1112A>C MANE Select	NP_000288.1:p.Glu371Ala
NR_156488.2:n.1211A>C