Canonical Allele Identifier: CA1474575883

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038493_88038494delinsTG , CM000666.2:g.88038493_88038494delinsTG	GRCh38
NC_000004.11:g.88959645_88959646delinsTG , CM000666.1:g.88959645_88959646delinsTG	GRCh37
NC_000004.10:g.89178669_89178670delinsTG	NCBI36
NG_008604.1:g.35826_35827delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1086_1087delinsTG MANE Select	ENSP00000237596.2:p.Asn362=
ENST00000237596.6:c.1086_1087delinsTG	ENSP00000237596.2:p.Asn362=
ENST00000506367.1:n.533_534delinsTG
NM_000297.3:c.1086_1087delinsTG	NP_000288.1:p.Asn362=
XM_011532028.1:c.1086_1087delinsTG	XP_011530330.1:p.Asn362=
XM_011532029.1:c.366_367delinsTG	XP_011530331.1:p.Asn122=
XM_011532030.1:c.246_247delinsTG	XP_011530332.1:p.Asn82=
XR_244632.2:n.1181_1182delinsTG
NR_156488.1:n.1173_1174delinsTG
XM_011532028.2:c.1086_1087delinsTG	XP_011530330.1:p.Asn362=
XM_011532030.2:c.246_247delinsTG	XP_011530332.1:p.Asn82=
NM_000297.4:c.1086_1087delinsTG MANE Select	NP_000288.1:p.Asn362=
NR_156488.2:n.1185_1186delinsTG