Canonical Allele Identifier: CA10604867
Gene: PANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284671
dbSNP Id: rs780551883
gnomAD v4: 20-3889410-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3889410G>T , CM000682.2:g.3889410G>T GRCh38
NC_000020.10:g.3870057G>T , CM000682.1:g.3870057G>T GRCh37
NC_000020.9:g.3818057G>T NCBI36
NG_008131.3:g.5572G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000610179.7:c.-21G>T MANE Select ENSP00000477429.2:n.-21G>T
ENST00000316562.9:c.310G>T ENSP00000313377.4:p.Glu104Ter
ENST00000336066.8:c.-21G>T ENSP00000477229.2:n.-21G>T
ENST00000610179.6:c.-21G>T ENSP00000477429.2:n.-21G>T
ENST00000643504.2:c.-21G>T ENSP00000495157.2:n.-21G>T
ENST00000316562.8:c.310G>T ENSP00000313377.4:p.Glu104Ter
ENST00000336066.7:c.-60G>T ENSP00000477229.1:n.-60G>T
ENST00000495692.5:c.-538+394G>T ENSP00000476745.1:n.-538+394G>T
ENST00000497424.5:c.-246+506G>T ENSP00000417609.1:n.-246+506G>T
NM_024960.4:c.-246+506G>T NP_079236.3:n.-246+506G>T
NM_153638.2:c.310G>T NP_705902.2:p.Glu104Ter
XM_005260836.3:c.-246+394G>T XP_005260893.3:n.-246+394G>T
XM_011529364.1:c.310G>T XP_011527666.1:p.Glu104Ter
XM_011529365.1:c.310G>T XP_011527667.1:p.Glu104Ter
NM_001324191.1:c.-732G>T NP_001311120.1:n.-732G>T
NM_001324192.1:c.310G>T NP_001311121.1:p.Glu104Ter
NM_024960.5:c.-246+506G>T NP_079236.3:n.-246+506G>T
NM_153638.3:c.310G>T NP_705902.2:p.Glu104Ter
NR_136715.1:n.477G>T
XM_005260836.4:c.-246+394G>T XP_005260893.3:n.-246+394G>T
XM_011529364.3:c.310G>T XP_011527666.1:p.Glu104Ter
XM_011529365.2:c.310G>T XP_011527667.1:p.Glu104Ter
XM_017028079.2:c.-538+394G>T XP_016883568.1:n.-538+394G>T
XM_024452002.1:c.-538+506G>T XP_024307770.1:n.-538+506G>T
XR_002958533.1:n.471G>T
NM_001324191.2:c.-732G>T NP_001311120.1:n.-732G>T
NM_024960.6:c.-246+506G>T NP_079236.3:n.-246+506G>T
NR_136715.2:n.24G>T
NM_001386393.1:c.-21G>T MANE Select NP_001373322.1:n.-21G>T
NM_153638.4:c.310G>T NP_705902.2:p.Glu104Ter