Canonical Allele Identifier: CA2346797864
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912588G= , CM000682.2:g.3912588G= GRCh38
NC_000020.10:g.3893235G= , CM000682.1:g.3893235G= GRCh37
NC_000020.9:g.3841235G= NCBI36
NG_008131.3:g.28750G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.1036G= MANE Select ENSP00000477429.2:p.Gly346=
ENST00000316562.9:c.1366G= ENSP00000313377.4:p.Gly456=
ENST00000336066.8:c.*377G= ENSP00000477229.2:n.*377G=
ENST00000610179.6:c.1036G= ENSP00000477429.2:p.Gly346=
ENST00000643504.2:c.*666G= ENSP00000495157.2:n.*666G=
ENST00000646394.1:c.863G=
ENST00000316562.8:c.1366G= ENSP00000313377.4:p.Gly456=
ENST00000336066.7:c.*377G= ENSP00000477229.1:n.*377G=
ENST00000464452.1:n.601G=
ENST00000495692.5:c.58G= ENSP00000476745.1:p.Gly20=
ENST00000497424.5:c.493G= ENSP00000417609.1:p.Gly165=
ENST00000610179.5:c.997G= ENSP00000477429.1:p.Gly333=
ENST00000621507.1:c.493G= ENSP00000481523.1:p.Gly165=
NM_024960.4:c.493G= NP_079236.3:p.Gly165=
NM_153638.2:c.1366G= NP_705902.2:p.Gly456=
NM_153640.2:c.493G= NP_705904.1:p.Gly165=
XM_005260835.2:c.751G= XP_005260892.1:p.Gly251=
XM_005260836.3:c.493G= XP_005260893.3:p.Gly165=
XM_006723631.1:c.493G= XP_006723694.1:p.Gly165=
XM_011529364.1:c.1235+1758G= XP_011527666.1:n.1235+1758G=
NM_001324191.1:c.493G= NP_001311120.1:p.Gly165=
NM_001324193.1:c.58G= NP_001311122.1:p.Gly20=
NM_024960.5:c.493G= NP_079236.3:p.Gly165=
NM_153638.3:c.1366G= NP_705902.2:p.Gly456=
NM_153640.3:c.493G= NP_705904.1:p.Gly165=
NR_136715.1:n.1390G=
XM_005260835.3:c.751G= XP_005260892.1:p.Gly251=
XM_005260836.4:c.493G= XP_005260893.3:p.Gly165=
XM_011529364.3:c.1235+1758G= XP_011527666.1:n.1235+1758G=
XM_017028077.2:c.58G= XP_016883566.1:p.Gly20=
XM_017028078.2:c.58G= XP_016883567.1:p.Gly20=
XM_017028079.2:c.58G= XP_016883568.1:p.Gly20=
XM_024452002.1:c.58G= XP_024307770.1:p.Gly20=
XR_002958533.1:n.2154G=
NM_001324191.2:c.493G= NP_001311120.1:p.Gly165=
NM_001324193.2:c.58G= NP_001311122.1:p.Gly20=
NM_024960.6:c.493G= NP_079236.3:p.Gly165=
NR_136715.2:n.937G=
NM_001386393.1:c.1036G= MANE Select NP_001373322.1:p.Gly346=
NM_153638.4:c.1366G= NP_705902.2:p.Gly456=
NM_153640.4:c.493G= NP_705904.1:p.Gly165=