Canonical Allele Identifier: CA357633289

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88959644A>T (hg19) ; chr4:g.88038492A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038492A>T , CM000666.2:g.88038492A>T	GRCh38
NC_000004.11:g.88959644A>T , CM000666.1:g.88959644A>T	GRCh37
NC_000004.10:g.89178668A>T	NCBI36
NG_008604.1:g.35825A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1085A>T MANE Select	ENSP00000237596.2:p.Asn362Ile
ENST00000237596.6:c.1085A>T	ENSP00000237596.2:p.Asn362Ile
ENST00000506367.1:n.532A>T
NM_000297.3:c.1085A>T	NP_000288.1:p.Asn362Ile
XM_011532028.1:c.1085A>T	XP_011530330.1:p.Asn362Ile
XM_011532029.1:c.365A>T	XP_011530331.1:p.Asn122Ile
XM_011532030.1:c.245A>T	XP_011530332.1:p.Asn82Ile
XR_244632.2:n.1180A>T
NR_156488.1:n.1172A>T
XM_011532028.2:c.1085A>T	XP_011530330.1:p.Asn362Ile
XM_011532030.2:c.245A>T	XP_011530332.1:p.Asn82Ile
NM_000297.4:c.1085A>T MANE Select	NP_000288.1:p.Asn362Ile
NR_156488.2:n.1184A>T