Canonical Allele Identifier: CA2346795541
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3907745_3907746delinsAT , CM000682.2:g.3907745_3907746delinsAT GRCh38
NC_000020.10:g.3888392_3888393delinsAT , CM000682.1:g.3888392_3888393delinsAT GRCh37
NC_000020.9:g.3836392_3836393delinsAT NCBI36
NG_008131.3:g.23907_23908delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.299-181_299-180delinsAT MANE Select ENSP00000477429.2:n.299-181_299-180delinsAT
ENST00000316562.9:c.629-181_629-180delinsAT ENSP00000313377.4:n.629-181_629-180delinsAT
ENST00000336066.8:c.299-181_299-180delinsAT ENSP00000477229.2:n.299-181_299-180delinsAT
ENST00000610179.6:c.299-181_299-180delinsAT ENSP00000477429.2:n.299-181_299-180delinsAT
ENST00000643504.2:c.*72-181_*72-180delinsAT ENSP00000495157.2:n.*72-181_*72-180delinsAT
ENST00000646394.1:c.126-181_126-180delinsAT
ENST00000316562.8:c.629-181_629-180delinsAT ENSP00000313377.4:n.629-181_629-180delinsAT
ENST00000336066.7:c.260-181_260-180delinsAT ENSP00000477229.1:n.260-181_260-180delinsAT
ENST00000471830.1:n.173-181_173-180delinsAT
ENST00000495692.5:c.-537-181_-537-180delinsAT ENSP00000476745.1:n.-537-181_-537-180delinsAT
ENST00000497424.5:c.-245-181_-245-180delinsAT ENSP00000417609.1:n.-245-181_-245-180delinsAT
ENST00000610179.5:c.260-181_260-180delinsAT ENSP00000477429.1:n.260-181_260-180delinsAT
ENST00000621507.1:c.-245-181_-245-180delinsAT ENSP00000481523.1:n.-245-181_-245-180delinsAT
NM_024960.4:c.-245-181_-245-180delinsAT NP_079236.3:n.-245-181_-245-180delinsAT
NM_153638.2:c.629-181_629-180delinsAT NP_705902.2:n.629-181_629-180delinsAT
NM_153640.2:c.-245-181_-245-180delinsAT NP_705904.1:n.-245-181_-245-180delinsAT
XM_005260835.2:c.14-181_14-180delinsAT XP_005260892.1:n.14-181_14-180delinsAT
XM_005260836.3:c.-245-181_-245-180delinsAT XP_005260893.3:n.-245-181_-245-180delinsAT
XM_006723631.1:c.-245-181_-245-180delinsAT XP_006723694.1:n.-245-181_-245-180delinsAT
XM_011529364.1:c.629-181_629-180delinsAT XP_011527666.1:n.629-181_629-180delinsAT
XM_011529365.1:c.629-181_629-180delinsAT XP_011527667.1:n.629-181_629-180delinsAT
NM_001324191.1:c.-245-181_-245-180delinsAT NP_001311120.1:n.-245-181_-245-180delinsAT
NM_001324192.1:c.629-181_629-180delinsAT NP_001311121.1:n.629-181_629-180delinsAT
NM_001324193.1:c.-537-181_-537-180delinsAT NP_001311122.1:n.-537-181_-537-180delinsAT
NM_024960.5:c.-245-181_-245-180delinsAT NP_079236.3:n.-245-181_-245-180delinsAT
NM_153638.3:c.629-181_629-180delinsAT NP_705902.2:n.629-181_629-180delinsAT
NM_153640.3:c.-245-181_-245-180delinsAT NP_705904.1:n.-245-181_-245-180delinsAT
NR_136715.1:n.796-181_796-180delinsAT
XM_005260835.3:c.14-181_14-180delinsAT XP_005260892.1:n.14-181_14-180delinsAT
XM_005260836.4:c.-245-181_-245-180delinsAT XP_005260893.3:n.-245-181_-245-180delinsAT
XM_011529364.3:c.629-181_629-180delinsAT XP_011527666.1:n.629-181_629-180delinsAT
XM_011529365.2:c.629-181_629-180delinsAT XP_011527667.1:n.629-181_629-180delinsAT
XM_017028077.2:c.-537-181_-537-180delinsAT XP_016883566.1:n.-537-181_-537-180delinsAT
XM_017028078.2:c.-537-181_-537-180delinsAT XP_016883567.1:n.-537-181_-537-180delinsAT
XM_017028079.2:c.-537-181_-537-180delinsAT XP_016883568.1:n.-537-181_-537-180delinsAT
XM_024452002.1:c.-537-181_-537-180delinsAT XP_024307770.1:n.-537-181_-537-180delinsAT
XR_002958533.1:n.790-181_790-180delinsAT
NM_001324191.2:c.-245-181_-245-180delinsAT NP_001311120.1:n.-245-181_-245-180delinsAT
NM_001324193.2:c.-537-181_-537-180delinsAT NP_001311122.1:n.-537-181_-537-180delinsAT
NM_024960.6:c.-245-181_-245-180delinsAT NP_079236.3:n.-245-181_-245-180delinsAT
NR_136715.2:n.343-181_343-180delinsAT
NM_001386393.1:c.299-181_299-180delinsAT MANE Select NP_001373322.1:n.299-181_299-180delinsAT
NM_153638.4:c.629-181_629-180delinsAT NP_705902.2:n.629-181_629-180delinsAT
NM_153640.4:c.-245-181_-245-180delinsAT NP_705904.1:n.-245-181_-245-180delinsAT