Canonical Allele Identifier: CA2736360618

Gene: PANK2

Linked Data

• dbSNP Id: rs2146859163

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3907919_3907922del , CM000682.2:g.3907919_3907922del	GRCh38
NC_000020.10:g.3888566_3888569del , CM000682.1:g.3888566_3888569del	GRCh37
NC_000020.9:g.3836566_3836569del	NCBI36
NG_008131.3:g.24081_24084del

Transcript Alleles

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