Canonical Allele Identifier: CA2346797843

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912538_3912539delinsCT , CM000682.2:g.3912538_3912539delinsCT	GRCh38
NC_000020.10:g.3893185_3893186delinsCT , CM000682.1:g.3893185_3893186delinsCT	GRCh37
NC_000020.9:g.3841185_3841186delinsCT	NCBI36
NG_008131.3:g.28700_28701delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000610179.7:c.986_987delinsCT MANE Select	ENSP00000477429.2:p.Ser329=
ENST00000316562.9:c.1316_1317delinsCT	ENSP00000313377.4:p.Ser439=
ENST00000336066.8:c.*327_*328delinsCT	ENSP00000477229.2:n.*327_*328delinsCT
ENST00000610179.6:c.986_987delinsCT	ENSP00000477429.2:p.Ser329=
ENST00000643504.2:c.*616_*617delinsCT	ENSP00000495157.2:n.*616_*617delinsCT
ENST00000646394.1:c.813_814delinsCT
ENST00000316562.8:c.1316_1317delinsCT	ENSP00000313377.4:p.Ser439=
ENST00000336066.7:c.*327_*328delinsCT	ENSP00000477229.1:n.*327_*328delinsCT
ENST00000464452.1:n.551_552delinsCT
ENST00000495692.5:c.8_9delinsCT	ENSP00000476745.1:p.Ser3=
ENST00000497424.5:c.443_444delinsCT	ENSP00000417609.1:p.Ser148=
ENST00000610179.5:c.947_948delinsCT	ENSP00000477429.1:p.Ser316=
ENST00000621507.1:c.443_444delinsCT	ENSP00000481523.1:p.Ser148=
NM_024960.4:c.443_444delinsCT	NP_079236.3:p.Ser148=
NM_153638.2:c.1316_1317delinsCT	NP_705902.2:p.Ser439=
NM_153640.2:c.443_444delinsCT	NP_705904.1:p.Ser148=
XM_005260835.2:c.701_702delinsCT	XP_005260892.1:p.Ser234=
XM_005260836.3:c.443_444delinsCT	XP_005260893.3:p.Ser148=
XM_006723631.1:c.443_444delinsCT	XP_006723694.1:p.Ser148=
XM_011529364.1:c.1235+1708_1235+1709delinsCT	XP_011527666.1:n.1235+1708_1235+1709delin...
NM_001324191.1:c.443_444delinsCT	NP_001311120.1:p.Ser148=
NM_001324193.1:c.8_9delinsCT	NP_001311122.1:p.Ser3=
NM_024960.5:c.443_444delinsCT	NP_079236.3:p.Ser148=
NM_153638.3:c.1316_1317delinsCT	NP_705902.2:p.Ser439=
NM_153640.3:c.443_444delinsCT	NP_705904.1:p.Ser148=
NR_136715.1:n.1340_1341delinsCT
XM_005260835.3:c.701_702delinsCT	XP_005260892.1:p.Ser234=
XM_005260836.4:c.443_444delinsCT	XP_005260893.3:p.Ser148=
XM_011529364.3:c.1235+1708_1235+1709delinsCT	XP_011527666.1:n.1235+1708_1235+1709delin...
XM_017028077.2:c.8_9delinsCT	XP_016883566.1:p.Ser3=
XM_017028078.2:c.8_9delinsCT	XP_016883567.1:p.Ser3=
XM_017028079.2:c.8_9delinsCT	XP_016883568.1:p.Ser3=
XM_024452002.1:c.8_9delinsCT	XP_024307770.1:p.Ser3=
XR_002958533.1:n.2104_2105delinsCT
NM_001324191.2:c.443_444delinsCT	NP_001311120.1:p.Ser148=
NM_001324193.2:c.8_9delinsCT	NP_001311122.1:p.Ser3=
NM_024960.6:c.443_444delinsCT	NP_079236.3:p.Ser148=
NR_136715.2:n.887_888delinsCT
NM_001386393.1:c.986_987delinsCT MANE Select	NP_001373322.1:p.Ser329=
NM_153638.4:c.1316_1317delinsCT	NP_705902.2:p.Ser439=
NM_153640.4:c.443_444delinsCT	NP_705904.1:p.Ser148=