Canonical Allele Identifier: CA2815082502

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912667_3912668insACA , CM000682.2:g.3912667_3912668insACA	GRCh38
NC_000020.10:g.3893314_3893315insACA , CM000682.1:g.3893314_3893315insACA	GRCh37
NC_000020.9:g.3841314_3841315insACA	NCBI36
NG_008131.3:g.28829_28830insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1082+33_1082+34insACA MANE Select	ENSP00000477429.2:n.1082+33_1082+34insACA
ENST00000316562.9:c.1412+33_1412+34insACA	ENSP00000313377.4:n.1412+33_1412+34insACA
ENST00000336066.8:c.*423+33_*423+34insACA	ENSP00000477229.2:n.*423+33_*423+34insACA
ENST00000610179.6:c.1082+33_1082+34insACA	ENSP00000477429.2:n.1082+33_1082+34insACA
ENST00000643504.2:c.*712+33_*712+34insACA	ENSP00000495157.2:n.*712+33_*712+34insACA
ENST00000646394.1:c.909+33_909+34insACA
ENST00000316562.8:c.1412+33_1412+34insACA	ENSP00000313377.4:n.1412+33_1412+34insACA
ENST00000336066.7:c.*423+33_*423+34insACA	ENSP00000477229.1:n.*423+33_*423+34insACA
ENST00000464452.1:n.647+33_647+34insACA
ENST00000495692.5:c.104+33_104+34insACA	ENSP00000476745.1:n.104+33_104+34insACA
ENST00000497424.5:c.539+33_539+34insACA	ENSP00000417609.1:n.539+33_539+34insACA
ENST00000610179.5:c.1043+33_1043+34insACA	ENSP00000477429.1:n.1043+33_1043+34insACA
ENST00000621507.1:c.539+33_539+34insACA	ENSP00000481523.1:n.539+33_539+34insACA
NM_024960.4:c.539+33_539+34insACA	NP_079236.3:n.539+33_539+34insACA
NM_153638.2:c.1412+33_1412+34insACA	NP_705902.2:n.1412+33_1412+34insACA
NM_153640.2:c.539+33_539+34insACA	NP_705904.1:n.539+33_539+34insACA
XM_005260835.2:c.797+33_797+34insACA	XP_005260892.1:n.797+33_797+34insACA
XM_005260836.3:c.539+33_539+34insACA	XP_005260893.3:n.539+33_539+34insACA
XM_006723631.1:c.539+33_539+34insACA	XP_006723694.1:n.539+33_539+34insACA
XM_011529364.1:c.1235+1837_1235+1838insACA	XP_011527666.1:n.1235+1837_1235+1838insACA
NM_001324191.1:c.539+33_539+34insACA	NP_001311120.1:n.539+33_539+34insACA
NM_001324193.1:c.104+33_104+34insACA	NP_001311122.1:n.104+33_104+34insACA
NM_024960.5:c.539+33_539+34insACA	NP_079236.3:n.539+33_539+34insACA
NM_153638.3:c.1412+33_1412+34insACA	NP_705902.2:n.1412+33_1412+34insACA
NM_153640.3:c.539+33_539+34insACA	NP_705904.1:n.539+33_539+34insACA
NR_136715.1:n.1436+33_1436+34insACA
XM_005260835.3:c.797+33_797+34insACA	XP_005260892.1:n.797+33_797+34insACA
XM_005260836.4:c.539+33_539+34insACA	XP_005260893.3:n.539+33_539+34insACA
XM_011529364.3:c.1235+1837_1235+1838insACA	XP_011527666.1:n.1235+1837_1235+1838insACA
XM_017028077.2:c.104+33_104+34insACA	XP_016883566.1:n.104+33_104+34insACA
XM_017028078.2:c.104+33_104+34insACA	XP_016883567.1:n.104+33_104+34insACA
XM_017028079.2:c.104+33_104+34insACA	XP_016883568.1:n.104+33_104+34insACA
XM_024452002.1:c.104+33_104+34insACA	XP_024307770.1:n.104+33_104+34insACA
XR_002958533.1:n.2200+33_2200+34insACA
NM_001324191.2:c.539+33_539+34insACA	NP_001311120.1:n.539+33_539+34insACA
NM_001324193.2:c.104+33_104+34insACA	NP_001311122.1:n.104+33_104+34insACA
NM_024960.6:c.539+33_539+34insACA	NP_079236.3:n.539+33_539+34insACA
NR_136715.2:n.983+33_983+34insACA
NM_001386393.1:c.1082+33_1082+34insACA MANE Select	NP_001373322.1:n.1082+33_1082+34insACA
NM_153638.4:c.1412+33_1412+34insACA	NP_705902.2:n.1412+33_1412+34insACA
NM_153640.4:c.539+33_539+34insACA	NP_705904.1:n.539+33_539+34insACA