Canonical Allele Identifier: CA2815082505

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912668_3912669insACT , CM000682.2:g.3912668_3912669insACT	GRCh38
NC_000020.10:g.3893315_3893316insACT , CM000682.1:g.3893315_3893316insACT	GRCh37
NC_000020.9:g.3841315_3841316insACT	NCBI36
NG_008131.3:g.28830_28831insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1082+34_1082+35insACT MANE Select	ENSP00000477429.2:n.1082+34_1082+35insACT
ENST00000316562.9:c.1412+34_1412+35insACT	ENSP00000313377.4:n.1412+34_1412+35insACT
ENST00000336066.8:c.*423+34_*423+35insACT	ENSP00000477229.2:n.*423+34_*423+35insACT
ENST00000610179.6:c.1082+34_1082+35insACT	ENSP00000477429.2:n.1082+34_1082+35insACT
ENST00000643504.2:c.*712+34_*712+35insACT	ENSP00000495157.2:n.*712+34_*712+35insACT
ENST00000646394.1:c.909+34_909+35insACT
ENST00000316562.8:c.1412+34_1412+35insACT	ENSP00000313377.4:n.1412+34_1412+35insACT
ENST00000336066.7:c.*423+34_*423+35insACT	ENSP00000477229.1:n.*423+34_*423+35insACT
ENST00000464452.1:n.647+34_647+35insACT
ENST00000495692.5:c.104+34_104+35insACT	ENSP00000476745.1:n.104+34_104+35insACT
ENST00000497424.5:c.539+34_539+35insACT	ENSP00000417609.1:n.539+34_539+35insACT
ENST00000610179.5:c.1043+34_1043+35insACT	ENSP00000477429.1:n.1043+34_1043+35insACT
ENST00000621507.1:c.539+34_539+35insACT	ENSP00000481523.1:n.539+34_539+35insACT
NM_024960.4:c.539+34_539+35insACT	NP_079236.3:n.539+34_539+35insACT
NM_153638.2:c.1412+34_1412+35insACT	NP_705902.2:n.1412+34_1412+35insACT
NM_153640.2:c.539+34_539+35insACT	NP_705904.1:n.539+34_539+35insACT
XM_005260835.2:c.797+34_797+35insACT	XP_005260892.1:n.797+34_797+35insACT
XM_005260836.3:c.539+34_539+35insACT	XP_005260893.3:n.539+34_539+35insACT
XM_006723631.1:c.539+34_539+35insACT	XP_006723694.1:n.539+34_539+35insACT
XM_011529364.1:c.1235+1838_1235+1839insACT	XP_011527666.1:n.1235+1838_1235+1839insACT
NM_001324191.1:c.539+34_539+35insACT	NP_001311120.1:n.539+34_539+35insACT
NM_001324193.1:c.104+34_104+35insACT	NP_001311122.1:n.104+34_104+35insACT
NM_024960.5:c.539+34_539+35insACT	NP_079236.3:n.539+34_539+35insACT
NM_153638.3:c.1412+34_1412+35insACT	NP_705902.2:n.1412+34_1412+35insACT
NM_153640.3:c.539+34_539+35insACT	NP_705904.1:n.539+34_539+35insACT
NR_136715.1:n.1436+34_1436+35insACT
XM_005260835.3:c.797+34_797+35insACT	XP_005260892.1:n.797+34_797+35insACT
XM_005260836.4:c.539+34_539+35insACT	XP_005260893.3:n.539+34_539+35insACT
XM_011529364.3:c.1235+1838_1235+1839insACT	XP_011527666.1:n.1235+1838_1235+1839insACT
XM_017028077.2:c.104+34_104+35insACT	XP_016883566.1:n.104+34_104+35insACT
XM_017028078.2:c.104+34_104+35insACT	XP_016883567.1:n.104+34_104+35insACT
XM_017028079.2:c.104+34_104+35insACT	XP_016883568.1:n.104+34_104+35insACT
XM_024452002.1:c.104+34_104+35insACT	XP_024307770.1:n.104+34_104+35insACT
XR_002958533.1:n.2200+34_2200+35insACT
NM_001324191.2:c.539+34_539+35insACT	NP_001311120.1:n.539+34_539+35insACT
NM_001324193.2:c.104+34_104+35insACT	NP_001311122.1:n.104+34_104+35insACT
NM_024960.6:c.539+34_539+35insACT	NP_079236.3:n.539+34_539+35insACT
NR_136715.2:n.983+34_983+35insACT
NM_001386393.1:c.1082+34_1082+35insACT MANE Select	NP_001373322.1:n.1082+34_1082+35insACT
NM_153638.4:c.1412+34_1412+35insACT	NP_705902.2:n.1412+34_1412+35insACT
NM_153640.4:c.539+34_539+35insACT	NP_705904.1:n.539+34_539+35insACT