Canonical Allele Identifier: CA440296991

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88929356A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88008204A>T , CM000666.2:g.88008204A>T	GRCh38
NC_000004.11:g.88929356A>T , CM000666.1:g.88929356A>T	GRCh37
NC_000004.10:g.89148380A>T	NCBI36
NG_008604.1:g.5537A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.471A>T MANE Select	ENSP00000237596.2:p.Arg157=
ENST00000237596.6:c.471A>T	ENSP00000237596.2:p.Arg157=
NM_000297.3:c.471A>T	NP_000288.1:p.Arg157=
XM_011532028.1:c.471A>T	XP_011530330.1:p.Arg157=
XR_244632.2:n.566A>T
NR_156488.1:n.558A>T
XM_011532028.2:c.471A>T	XP_011530330.1:p.Arg157=
NM_000297.4:c.471A>T MANE Select	NP_000288.1:p.Arg157=
NR_156488.2:n.570A>T