Canonical Allele Identifier: CA408117867
Gene: PANK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912597G>T , CM000682.2:g.3912597G>T GRCh38
NC_000020.10:g.3893244G>T , CM000682.1:g.3893244G>T GRCh37
NC_000020.9:g.3841244G>T NCBI36
NG_008131.3:g.28759G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.1045G>T MANE Select ENSP00000477429.2:p.Glu349Ter
ENST00000316562.9:c.1375G>T ENSP00000313377.4:p.Glu459Ter
ENST00000336066.8:c.*386G>T ENSP00000477229.2:n.*386G>T
ENST00000610179.6:c.1045G>T ENSP00000477429.2:p.Glu349Ter
ENST00000643504.2:c.*675G>T ENSP00000495157.2:n.*675G>T
ENST00000646394.1:c.872G>T
ENST00000316562.8:c.1375G>T ENSP00000313377.4:p.Glu459Ter
ENST00000336066.7:c.*386G>T ENSP00000477229.1:n.*386G>T
ENST00000464452.1:n.610G>T
ENST00000495692.5:c.67G>T ENSP00000476745.1:p.Glu23Ter
ENST00000497424.5:c.502G>T ENSP00000417609.1:p.Glu168Ter
ENST00000610179.5:c.1006G>T ENSP00000477429.1:p.Glu336Ter
ENST00000621507.1:c.502G>T ENSP00000481523.1:p.Glu168Ter
NM_024960.4:c.502G>T NP_079236.3:p.Glu168Ter
NM_153638.2:c.1375G>T NP_705902.2:p.Glu459Ter
NM_153640.2:c.502G>T NP_705904.1:p.Glu168Ter
XM_005260835.2:c.760G>T XP_005260892.1:p.Glu254Ter
XM_005260836.3:c.502G>T XP_005260893.3:p.Glu168Ter
XM_006723631.1:c.502G>T XP_006723694.1:p.Glu168Ter
XM_011529364.1:c.1235+1767G>T XP_011527666.1:n.1235+1767G>T
NM_001324191.1:c.502G>T NP_001311120.1:p.Glu168Ter
NM_001324193.1:c.67G>T NP_001311122.1:p.Glu23Ter
NM_024960.5:c.502G>T NP_079236.3:p.Glu168Ter
NM_153638.3:c.1375G>T NP_705902.2:p.Glu459Ter
NM_153640.3:c.502G>T NP_705904.1:p.Glu168Ter
NR_136715.1:n.1399G>T
XM_005260835.3:c.760G>T XP_005260892.1:p.Glu254Ter
XM_005260836.4:c.502G>T XP_005260893.3:p.Glu168Ter
XM_011529364.3:c.1235+1767G>T XP_011527666.1:n.1235+1767G>T
XM_017028077.2:c.67G>T XP_016883566.1:p.Glu23Ter
XM_017028078.2:c.67G>T XP_016883567.1:p.Glu23Ter
XM_017028079.2:c.67G>T XP_016883568.1:p.Glu23Ter
XM_024452002.1:c.67G>T XP_024307770.1:p.Glu23Ter
XR_002958533.1:n.2163G>T
NM_001324191.2:c.502G>T NP_001311120.1:p.Glu168Ter
NM_001324193.2:c.67G>T NP_001311122.1:p.Glu23Ter
NM_024960.6:c.502G>T NP_079236.3:p.Glu168Ter
NR_136715.2:n.946G>T
NM_001386393.1:c.1045G>T MANE Select NP_001373322.1:p.Glu349Ter
NM_153638.4:c.1375G>T NP_705902.2:p.Glu459Ter
NM_153640.4:c.502G>T NP_705904.1:p.Glu168Ter