Canonical Allele Identifier: CA2346797850
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912553C= , CM000682.2:g.3912553C= GRCh38
NC_000020.10:g.3893200C= , CM000682.1:g.3893200C= GRCh37
NC_000020.9:g.3841200C= NCBI36
NG_008131.3:g.28715C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.1001C= MANE Select ENSP00000477429.2:p.Thr334=
ENST00000316562.9:c.1331C= ENSP00000313377.4:p.Thr444=
ENST00000336066.8:c.*342C= ENSP00000477229.2:n.*342C=
ENST00000610179.6:c.1001C= ENSP00000477429.2:p.Thr334=
ENST00000643504.2:c.*631C= ENSP00000495157.2:n.*631C=
ENST00000646394.1:c.828C=
ENST00000316562.8:c.1331C= ENSP00000313377.4:p.Thr444=
ENST00000336066.7:c.*342C= ENSP00000477229.1:n.*342C=
ENST00000464452.1:n.566C=
ENST00000495692.5:c.23C= ENSP00000476745.1:p.Thr8=
ENST00000497424.5:c.458C= ENSP00000417609.1:p.Thr153=
ENST00000610179.5:c.962C= ENSP00000477429.1:p.Thr321=
ENST00000621507.1:c.458C= ENSP00000481523.1:p.Thr153=
NM_024960.4:c.458C= NP_079236.3:p.Thr153=
NM_153638.2:c.1331C= NP_705902.2:p.Thr444=
NM_153640.2:c.458C= NP_705904.1:p.Thr153=
XM_005260835.2:c.716C= XP_005260892.1:p.Thr239=
XM_005260836.3:c.458C= XP_005260893.3:p.Thr153=
XM_006723631.1:c.458C= XP_006723694.1:p.Thr153=
XM_011529364.1:c.1235+1723C= XP_011527666.1:n.1235+1723C=
NM_001324191.1:c.458C= NP_001311120.1:p.Thr153=
NM_001324193.1:c.23C= NP_001311122.1:p.Thr8=
NM_024960.5:c.458C= NP_079236.3:p.Thr153=
NM_153638.3:c.1331C= NP_705902.2:p.Thr444=
NM_153640.3:c.458C= NP_705904.1:p.Thr153=
NR_136715.1:n.1355C=
XM_005260835.3:c.716C= XP_005260892.1:p.Thr239=
XM_005260836.4:c.458C= XP_005260893.3:p.Thr153=
XM_011529364.3:c.1235+1723C= XP_011527666.1:n.1235+1723C=
XM_017028077.2:c.23C= XP_016883566.1:p.Thr8=
XM_017028078.2:c.23C= XP_016883567.1:p.Thr8=
XM_017028079.2:c.23C= XP_016883568.1:p.Thr8=
XM_024452002.1:c.23C= XP_024307770.1:p.Thr8=
XR_002958533.1:n.2119C=
NM_001324191.2:c.458C= NP_001311120.1:p.Thr153=
NM_001324193.2:c.23C= NP_001311122.1:p.Thr8=
NM_024960.6:c.458C= NP_079236.3:p.Thr153=
NR_136715.2:n.902C=
NM_001386393.1:c.1001C= MANE Select NP_001373322.1:p.Thr334=
NM_153638.4:c.1331C= NP_705902.2:p.Thr444=
NM_153640.4:c.458C= NP_705904.1:p.Thr153=