Canonical Allele Identifier: CA2346797831
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912503C= , CM000682.2:g.3912503C= GRCh38
NC_000020.10:g.3893150C= , CM000682.1:g.3893150C= GRCh37
NC_000020.9:g.3841150C= NCBI36
NG_008131.3:g.28665C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.951C= MANE Select ENSP00000477429.2:p.Gly317=
ENST00000316562.9:c.1281C= ENSP00000313377.4:p.Gly427=
ENST00000336066.8:c.*292C= ENSP00000477229.2:n.*292C=
ENST00000610179.6:c.951C= ENSP00000477429.2:p.Gly317=
ENST00000643504.2:c.*581C= ENSP00000495157.2:n.*581C=
ENST00000646394.1:c.778C=
ENST00000316562.8:c.1281C= ENSP00000313377.4:p.Gly427=
ENST00000336066.7:c.*292C= ENSP00000477229.1:n.*292C=
ENST00000464452.1:n.516C=
ENST00000495692.5:c.-28C= ENSP00000476745.1:n.-28C=
ENST00000497424.5:c.408C= ENSP00000417609.1:p.Gly136=
ENST00000610179.5:c.912C= ENSP00000477429.1:p.Gly304=
ENST00000621507.1:c.408C= ENSP00000481523.1:p.Gly136=
NM_024960.4:c.408C= NP_079236.3:p.Gly136=
NM_153638.2:c.1281C= NP_705902.2:p.Gly427=
NM_153640.2:c.408C= NP_705904.1:p.Gly136=
XM_005260835.2:c.666C= XP_005260892.1:p.Gly222=
XM_005260836.3:c.408C= XP_005260893.3:p.Gly136=
XM_006723631.1:c.408C= XP_006723694.1:p.Gly136=
XM_011529364.1:c.1235+1673C= XP_011527666.1:n.1235+1673C=
NM_001324191.1:c.408C= NP_001311120.1:p.Gly136=
NM_001324193.1:c.-28C= NP_001311122.1:n.-28C=
NM_024960.5:c.408C= NP_079236.3:p.Gly136=
NM_153638.3:c.1281C= NP_705902.2:p.Gly427=
NM_153640.3:c.408C= NP_705904.1:p.Gly136=
NR_136715.1:n.1305C=
XM_005260835.3:c.666C= XP_005260892.1:p.Gly222=
XM_005260836.4:c.408C= XP_005260893.3:p.Gly136=
XM_011529364.3:c.1235+1673C= XP_011527666.1:n.1235+1673C=
XM_017028077.2:c.-28C= XP_016883566.1:n.-28C=
XM_017028078.2:c.-28C= XP_016883567.1:n.-28C=
XM_017028079.2:c.-28C= XP_016883568.1:n.-28C=
XM_024452002.1:c.-28C= XP_024307770.1:n.-28C=
XR_002958533.1:n.2069C=
NM_001324191.2:c.408C= NP_001311120.1:p.Gly136=
NM_001324193.2:c.-28C= NP_001311122.1:n.-28C=
NM_024960.6:c.408C= NP_079236.3:p.Gly136=
NR_136715.2:n.852C=
NM_001386393.1:c.951C= MANE Select NP_001373322.1:p.Gly317=
NM_153638.4:c.1281C= NP_705902.2:p.Gly427=
NM_153640.4:c.408C= NP_705904.1:p.Gly136=