Canonical Allele Identifier: CA9750857

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3916913_3916914insCCCCCT , CM000682.2:g.3916913_3916914insCCCCCT	GRCh38
NC_000020.10:g.3897560_3897561insCCCCCT , CM000682.1:g.3897560_3897561insCCCCCT	GRCh37
NC_000020.9:g.3845560_3845561insCCCCCT	NCBI36
NG_008131.3:g.33075_33076insCCCCCT

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.1083-14_1083-13insCCCCCT MANE Select	NP_001373322.1:n.1083-14_1083-13insCCCCCT
ENST00000610179.7:c.1083-14_1083-13insCCCCCT MANE Select	ENSP00000477429.2:n.1083-14_1083-13insCCCCCT
NM_001324191.1:c.540-14_540-13insCCCCCT	NP_001311120.1:n.540-14_540-13insCCCCCT
NM_001324191.2:c.540-14_540-13insCCCCCT	NP_001311120.1:n.540-14_540-13insCCCCCT
NM_001324193.1:c.105-14_105-13insCCCCCT	NP_001311122.1:n.105-14_105-13insCCCCCT
NM_001324193.2:c.105-14_105-13insCCCCCT	NP_001311122.1:n.105-14_105-13insCCCCCT
NM_024960.4:c.540-14_540-13insCCCCCT	NP_079236.3:n.540-14_540-13insCCCCCT
NM_024960.5:c.540-14_540-13insCCCCCT	NP_079236.3:n.540-14_540-13insCCCCCT
NM_024960.6:c.540-14_540-13insCCCCCT	NP_079236.3:n.540-14_540-13insCCCCCT
NM_153638.2:c.1413-14_1413-13insCCCCCT	NP_705902.2:n.1413-14_1413-13insCCCCCT
NM_153638.3:c.1413-14_1413-13insCCCCCT	NP_705902.2:n.1413-14_1413-13insCCCCCT
NM_153638.4:c.1413-14_1413-13insCCCCCT	NP_705902.2:n.1413-14_1413-13insCCCCCT
NM_153640.2:c.540-14_540-13insCCCCCT	NP_705904.1:n.540-14_540-13insCCCCCT
NM_153640.3:c.540-14_540-13insCCCCCT	NP_705904.1:n.540-14_540-13insCCCCCT
NM_153640.4:c.540-14_540-13insCCCCCT	NP_705904.1:n.540-14_540-13insCCCCCT
NR_136715.1:n.1437-14_1437-13insCCCCCT
NR_136715.2:n.984-14_984-13insCCCCCT
ENST00000316562.8:c.1413-14_1413-13insCCCCCT	ENSP00000313377.4:n.1413-14_1413-13insCCCCCT
ENST00000316562.9:c.1413-14_1413-13insCCCCCT	ENSP00000313377.4:n.1413-14_1413-13insCCCCCT
ENST00000336066.7:c.*424-14_*424-13insCCCCCT	ENSP00000477229.1:n.*424-14_*424-13insCCCCCT
ENST00000336066.8:c.*424-14_*424-13insCCCCCT	ENSP00000477229.2:n.*424-14_*424-13insCCCCCT
ENST00000464452.1:n.648-14_648-13insCCCCCT
ENST00000495692.5:c.105-14_105-13insCCCCCT	ENSP00000476745.1:n.105-14_105-13insCCCCCT
ENST00000497424.5:c.540-14_540-13insCCCCCT	ENSP00000417609.1:n.540-14_540-13insCCCCCT
ENST00000610179.5:c.1044-14_1044-13insCCCCCT	ENSP00000477429.1:n.1044-14_1044-13insCCCCCT
ENST00000610179.6:c.1083-14_1083-13insCCCCCT	ENSP00000477429.2:n.1083-14_1083-13insCCCCCT
ENST00000621507.1:c.540-14_540-13insCCCCCT	ENSP00000481523.1:n.540-14_540-13insCCCCCT
ENST00000643504.2:c.*713-14_*713-13insCCCCCT	ENSP00000495157.2:n.*713-14_*713-13insCCCCCT
ENST00000646394.1:c.910-14_910-13insCCCCCT
XM_005260835.2:c.798-14_798-13insCCCCCT	XP_005260892.1:n.798-14_798-13insCCCCCT
XM_005260835.3:c.798-14_798-13insCCCCCT	XP_005260892.1:n.798-14_798-13insCCCCCT
XM_005260836.3:c.540-14_540-13insCCCCCT	XP_005260893.3:n.540-14_540-13insCCCCCT
XM_005260836.4:c.540-14_540-13insCCCCCT	XP_005260893.3:n.540-14_540-13insCCCCCT
XM_006723631.1:c.540-14_540-13insCCCCCT	XP_006723694.1:n.540-14_540-13insCCCCCT
XM_011529364.1:c.1236-14_1236-13insCCCCCT	XP_011527666.1:n.1236-14_1236-13insCCCCCT
XM_011529364.3:c.1236-14_1236-13insCCCCCT	XP_011527666.1:n.1236-14_1236-13insCCCCCT
XM_017028077.2:c.105-14_105-13insCCCCCT	XP_016883566.1:n.105-14_105-13insCCCCCT
XM_017028078.2:c.105-14_105-13insCCCCCT	XP_016883567.1:n.105-14_105-13insCCCCCT
XM_017028079.2:c.105-14_105-13insCCCCCT	XP_016883568.1:n.105-14_105-13insCCCCCT
XM_024452002.1:c.105-14_105-13insCCCCCT	XP_024307770.1:n.105-14_105-13insCCCCCT
XR_002958533.1:n.2201-14_2201-13insCCCCCT