Canonical Allele Identifier: CA2346797837
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912514T= , CM000682.2:g.3912514T= GRCh38
NC_000020.10:g.3893161T= , CM000682.1:g.3893161T= GRCh37
NC_000020.9:g.3841161T= NCBI36
NG_008131.3:g.28676T=

Transcript Alleles

HGVS Amino-acid change
ENST00000610179.7:c.962T= MANE Select ENSP00000477429.2:p.Phe321=
ENST00000316562.9:c.1292T= ENSP00000313377.4:p.Phe431=
ENST00000336066.8:c.*303T= ENSP00000477229.2:n.*303T=
ENST00000610179.6:c.962T= ENSP00000477429.2:p.Phe321=
ENST00000643504.2:c.*592T= ENSP00000495157.2:n.*592T=
ENST00000646394.1:c.789T=
ENST00000316562.8:c.1292T= ENSP00000313377.4:p.Phe431=
ENST00000336066.7:c.*303T= ENSP00000477229.1:n.*303T=
ENST00000464452.1:n.527T=
ENST00000495692.5:c.-17T= ENSP00000476745.1:n.-17T=
ENST00000497424.5:c.419T= ENSP00000417609.1:p.Phe140=
ENST00000610179.5:c.923T= ENSP00000477429.1:p.Phe308=
ENST00000621507.1:c.419T= ENSP00000481523.1:p.Phe140=
NM_024960.4:c.419T= NP_079236.3:p.Phe140=
NM_153638.2:c.1292T= NP_705902.2:p.Phe431=
NM_153640.2:c.419T= NP_705904.1:p.Phe140=
XM_005260835.2:c.677T= XP_005260892.1:p.Phe226=
XM_005260836.3:c.419T= XP_005260893.3:p.Phe140=
XM_006723631.1:c.419T= XP_006723694.1:p.Phe140=
XM_011529364.1:c.1235+1684T= XP_011527666.1:n.1235+1684T=
NM_001324191.1:c.419T= NP_001311120.1:p.Phe140=
NM_001324193.1:c.-17T= NP_001311122.1:n.-17T=
NM_024960.5:c.419T= NP_079236.3:p.Phe140=
NM_153638.3:c.1292T= NP_705902.2:p.Phe431=
NM_153640.3:c.419T= NP_705904.1:p.Phe140=
NR_136715.1:n.1316T=
XM_005260835.3:c.677T= XP_005260892.1:p.Phe226=
XM_005260836.4:c.419T= XP_005260893.3:p.Phe140=
XM_011529364.3:c.1235+1684T= XP_011527666.1:n.1235+1684T=
XM_017028077.2:c.-17T= XP_016883566.1:n.-17T=
XM_017028078.2:c.-17T= XP_016883567.1:n.-17T=
XM_017028079.2:c.-17T= XP_016883568.1:n.-17T=
XM_024452002.1:c.-17T= XP_024307770.1:n.-17T=
XR_002958533.1:n.2080T=
NM_001324191.2:c.419T= NP_001311120.1:p.Phe140=
NM_001324193.2:c.-17T= NP_001311122.1:n.-17T=
NM_024960.6:c.419T= NP_079236.3:p.Phe140=
NR_136715.2:n.863T=
NM_001386393.1:c.962T= MANE Select NP_001373322.1:p.Phe321=
NM_153638.4:c.1292T= NP_705902.2:p.Phe431=
NM_153640.4:c.419T= NP_705904.1:p.Phe140=