Canonical Allele Identifier: CA2346795569

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3907811_3907812delinsGC , CM000682.2:g.3907811_3907812delinsGC	GRCh38
NC_000020.10:g.3888458_3888459delinsGC , CM000682.1:g.3888458_3888459delinsGC	GRCh37
NC_000020.9:g.3836458_3836459delinsGC	NCBI36
NG_008131.3:g.23973_23974delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.299-115_299-114delinsGC MANE Select	ENSP00000477429.2:n.299-115_299-114delinsGC
ENST00000316562.9:c.629-115_629-114delinsGC	ENSP00000313377.4:n.629-115_629-114delinsGC
ENST00000336066.8:c.299-115_299-114delinsGC	ENSP00000477229.2:n.299-115_299-114delinsGC
ENST00000610179.6:c.299-115_299-114delinsGC	ENSP00000477429.2:n.299-115_299-114delinsGC
ENST00000643504.2:c.*72-115_*72-114delinsGC	ENSP00000495157.2:n.*72-115_*72-114delinsGC
ENST00000646394.1:c.126-115_126-114delinsGC
ENST00000316562.8:c.629-115_629-114delinsGC	ENSP00000313377.4:n.629-115_629-114delinsGC
ENST00000336066.7:c.260-115_260-114delinsGC	ENSP00000477229.1:n.260-115_260-114delinsGC
ENST00000471830.1:n.173-115_173-114delinsGC
ENST00000495692.5:c.-537-115_-537-114delinsGC	ENSP00000476745.1:n.-537-115_-537-114delinsGC
ENST00000497424.5:c.-245-115_-245-114delinsGC	ENSP00000417609.1:n.-245-115_-245-114delinsGC
ENST00000610179.5:c.260-115_260-114delinsGC	ENSP00000477429.1:n.260-115_260-114delinsGC
ENST00000621507.1:c.-245-115_-245-114delinsGC	ENSP00000481523.1:n.-245-115_-245-114delinsGC
NM_024960.4:c.-245-115_-245-114delinsGC	NP_079236.3:n.-245-115_-245-114delinsGC
NM_153638.2:c.629-115_629-114delinsGC	NP_705902.2:n.629-115_629-114delinsGC
NM_153640.2:c.-245-115_-245-114delinsGC	NP_705904.1:n.-245-115_-245-114delinsGC
XM_005260835.2:c.14-115_14-114delinsGC	XP_005260892.1:n.14-115_14-114delinsGC
XM_005260836.3:c.-245-115_-245-114delinsGC	XP_005260893.3:n.-245-115_-245-114delinsGC
XM_006723631.1:c.-245-115_-245-114delinsGC	XP_006723694.1:n.-245-115_-245-114delinsGC
XM_011529364.1:c.629-115_629-114delinsGC	XP_011527666.1:n.629-115_629-114delinsGC
XM_011529365.1:c.629-115_629-114delinsGC	XP_011527667.1:n.629-115_629-114delinsGC
NM_001324191.1:c.-245-115_-245-114delinsGC	NP_001311120.1:n.-245-115_-245-114delinsGC
NM_001324192.1:c.629-115_629-114delinsGC	NP_001311121.1:n.629-115_629-114delinsGC
NM_001324193.1:c.-537-115_-537-114delinsGC	NP_001311122.1:n.-537-115_-537-114delinsGC
NM_024960.5:c.-245-115_-245-114delinsGC	NP_079236.3:n.-245-115_-245-114delinsGC
NM_153638.3:c.629-115_629-114delinsGC	NP_705902.2:n.629-115_629-114delinsGC
NM_153640.3:c.-245-115_-245-114delinsGC	NP_705904.1:n.-245-115_-245-114delinsGC
NR_136715.1:n.796-115_796-114delinsGC
XM_005260835.3:c.14-115_14-114delinsGC	XP_005260892.1:n.14-115_14-114delinsGC
XM_005260836.4:c.-245-115_-245-114delinsGC	XP_005260893.3:n.-245-115_-245-114delinsGC
XM_011529364.3:c.629-115_629-114delinsGC	XP_011527666.1:n.629-115_629-114delinsGC
XM_011529365.2:c.629-115_629-114delinsGC	XP_011527667.1:n.629-115_629-114delinsGC
XM_017028077.2:c.-537-115_-537-114delinsGC	XP_016883566.1:n.-537-115_-537-114delinsGC
XM_017028078.2:c.-537-115_-537-114delinsGC	XP_016883567.1:n.-537-115_-537-114delinsGC
XM_017028079.2:c.-537-115_-537-114delinsGC	XP_016883568.1:n.-537-115_-537-114delinsGC
XM_024452002.1:c.-537-115_-537-114delinsGC	XP_024307770.1:n.-537-115_-537-114delinsGC
XR_002958533.1:n.790-115_790-114delinsGC
NM_001324191.2:c.-245-115_-245-114delinsGC	NP_001311120.1:n.-245-115_-245-114delinsGC
NM_001324193.2:c.-537-115_-537-114delinsGC	NP_001311122.1:n.-537-115_-537-114delinsGC
NM_024960.6:c.-245-115_-245-114delinsGC	NP_079236.3:n.-245-115_-245-114delinsGC
NR_136715.2:n.343-115_343-114delinsGC
NM_001386393.1:c.299-115_299-114delinsGC MANE Select	NP_001373322.1:n.299-115_299-114delinsGC
NM_153638.4:c.629-115_629-114delinsGC	NP_705902.2:n.629-115_629-114delinsGC
NM_153640.4:c.-245-115_-245-114delinsGC	NP_705904.1:n.-245-115_-245-114delinsGC