Canonical Allele Identifier: CA2346797867
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912593C= , CM000682.2:g.3912593C= GRCh38
NC_000020.10:g.3893240C= , CM000682.1:g.3893240C= GRCh37
NC_000020.9:g.3841240C= NCBI36
NG_008131.3:g.28755C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.1041C= MANE Select ENSP00000477429.2:p.Asp347=
ENST00000316562.9:c.1371C= ENSP00000313377.4:p.Asp457=
ENST00000336066.8:c.*382C= ENSP00000477229.2:n.*382C=
ENST00000610179.6:c.1041C= ENSP00000477429.2:p.Asp347=
ENST00000643504.2:c.*671C= ENSP00000495157.2:n.*671C=
ENST00000646394.1:c.868C=
ENST00000316562.8:c.1371C= ENSP00000313377.4:p.Asp457=
ENST00000336066.7:c.*382C= ENSP00000477229.1:n.*382C=
ENST00000464452.1:n.606C=
ENST00000495692.5:c.63C= ENSP00000476745.1:p.Asp21=
ENST00000497424.5:c.498C= ENSP00000417609.1:p.Asp166=
ENST00000610179.5:c.1002C= ENSP00000477429.1:p.Asp334=
ENST00000621507.1:c.498C= ENSP00000481523.1:p.Asp166=
NM_024960.4:c.498C= NP_079236.3:p.Asp166=
NM_153638.2:c.1371C= NP_705902.2:p.Asp457=
NM_153640.2:c.498C= NP_705904.1:p.Asp166=
XM_005260835.2:c.756C= XP_005260892.1:p.Asp252=
XM_005260836.3:c.498C= XP_005260893.3:p.Asp166=
XM_006723631.1:c.498C= XP_006723694.1:p.Asp166=
XM_011529364.1:c.1235+1763C= XP_011527666.1:n.1235+1763C=
NM_001324191.1:c.498C= NP_001311120.1:p.Asp166=
NM_001324193.1:c.63C= NP_001311122.1:p.Asp21=
NM_024960.5:c.498C= NP_079236.3:p.Asp166=
NM_153638.3:c.1371C= NP_705902.2:p.Asp457=
NM_153640.3:c.498C= NP_705904.1:p.Asp166=
NR_136715.1:n.1395C=
XM_005260835.3:c.756C= XP_005260892.1:p.Asp252=
XM_005260836.4:c.498C= XP_005260893.3:p.Asp166=
XM_011529364.3:c.1235+1763C= XP_011527666.1:n.1235+1763C=
XM_017028077.2:c.63C= XP_016883566.1:p.Asp21=
XM_017028078.2:c.63C= XP_016883567.1:p.Asp21=
XM_017028079.2:c.63C= XP_016883568.1:p.Asp21=
XM_024452002.1:c.63C= XP_024307770.1:p.Asp21=
XR_002958533.1:n.2159C=
NM_001324191.2:c.498C= NP_001311120.1:p.Asp166=
NM_001324193.2:c.63C= NP_001311122.1:p.Asp21=
NM_024960.6:c.498C= NP_079236.3:p.Asp166=
NR_136715.2:n.942C=
NM_001386393.1:c.1041C= MANE Select NP_001373322.1:p.Asp347=
NM_153638.4:c.1371C= NP_705902.2:p.Asp457=
NM_153640.4:c.498C= NP_705904.1:p.Asp166=