Canonical Allele Identifier: CA357618350
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046642G>C , CM000666.2:g.88046642G>C GRCh38
NC_000004.11:g.88967794G>C , CM000666.1:g.88967794G>C GRCh37
NC_000004.10:g.89186818G>C NCBI36
NG_008604.1:g.43975G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1320G>C MANE Select ENSP00000237596.2:p.Arg440Ser
ENST00000237596.6:c.1320G>C ENSP00000237596.2:p.Arg440Ser
ENST00000508588.5:c.-199+3185G>C ENSP00000427131.1:n.-199+3185G>C
NM_000297.3:c.1320G>C NP_000288.1:p.Arg440Ser
XM_011532028.1:c.1095G>C XP_011530330.1:p.Ala365=
XM_011532029.1:c.600G>C XP_011530331.1:p.Arg200Ser
XM_011532030.1:c.480G>C XP_011530332.1:p.Arg160Ser
XR_244632.2:n.1415G>C
NR_156488.1:n.1407G>C
XM_011532028.2:c.1095G>C XP_011530330.1:p.Ala365=
XM_011532030.2:c.480G>C XP_011530332.1:p.Arg160Ser
NM_000297.4:c.1320G>C MANE Select NP_000288.1:p.Arg440Ser
NR_156488.2:n.1419G>C