Canonical Allele Identifier: CA440263329

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967974A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046822A>C , CM000666.2:g.88046822A>C	GRCh38
NC_000004.11:g.88967974A>C , CM000666.1:g.88967974A>C	GRCh37
NC_000004.10:g.89186998A>C	NCBI36
NG_008604.1:g.44155A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1500A>C MANE Select	ENSP00000237596.2:p.Leu500=
ENST00000237596.6:c.1500A>C	ENSP00000237596.2:p.Leu500=
ENST00000508588.5:c.-199+3365A>C	ENSP00000427131.1:n.-199+3365A>C
NM_000297.3:c.1500A>C	NP_000288.1:p.Leu500=
XM_011532028.1:c.1275A>C	XP_011530330.1:p.Leu425=
XM_011532029.1:c.780A>C	XP_011530331.1:p.Leu260=
XM_011532030.1:c.660A>C	XP_011530332.1:p.Leu220=
XR_244632.2:n.1595A>C
NR_156488.1:n.1587A>C
XM_011532028.2:c.1275A>C	XP_011530330.1:p.Leu425=
XM_011532030.2:c.660A>C	XP_011530332.1:p.Leu220=
NM_000297.4:c.1500A>C MANE Select	NP_000288.1:p.Leu500=
NR_156488.2:n.1599A>C