Canonical Allele Identifier: CA357619647

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88967971A>T (hg19) ; chr4:g.88046819A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88046819A>T , CM000666.2:g.88046819A>T	GRCh38
NC_000004.11:g.88967971A>T , CM000666.1:g.88967971A>T	GRCh37
NC_000004.10:g.89186995A>T	NCBI36
NG_008604.1:g.44152A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.1497A>T MANE Select	ENSP00000237596.2:p.Lys499Asn
ENST00000237596.6:c.1497A>T	ENSP00000237596.2:p.Lys499Asn
ENST00000508588.5:c.-199+3362A>T	ENSP00000427131.1:n.-199+3362A>T
NM_000297.3:c.1497A>T	NP_000288.1:p.Lys499Asn
XM_011532028.1:c.1272A>T	XP_011530330.1:p.Lys424Asn
XM_011532029.1:c.777A>T	XP_011530331.1:p.Lys259Asn
XM_011532030.1:c.657A>T	XP_011530332.1:p.Lys219Asn
XR_244632.2:n.1592A>T
NR_156488.1:n.1584A>T
XM_011532028.2:c.1272A>T	XP_011530330.1:p.Lys424Asn
XM_011532030.2:c.657A>T	XP_011530332.1:p.Lys219Asn
NM_000297.4:c.1497A>T MANE Select	NP_000288.1:p.Lys499Asn
NR_156488.2:n.1596A>T