Canonical Allele Identifier: CA2346800332

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3916931_3916938delinsGGAAACAT , CM000682.2:g.3916931_3916938delinsGGAAACAT	GRCh38
NC_000020.10:g.3897578_3897585delinsGGAAACAT , CM000682.1:g.3897578_3897585delinsGGAAACAT	GRCh37
NC_000020.9:g.3845578_3845585delinsGGAAACAT	NCBI36
NG_008131.3:g.33093_33100delinsGGAAACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1087_1094delinsGGAAACAT MANE Select	ENSP00000477429.2:p.Gly363=
ENST00000316562.9:c.1417_1424delinsGGAAACAT	ENSP00000313377.4:p.Gly473=
ENST00000336066.8:c.*428_*435delinsGGAAACAT	ENSP00000477229.2:n.*428_*435delinsGGAAACAT
ENST00000610179.6:c.1087_1094delinsGGAAACAT	ENSP00000477429.2:p.Gly363=
ENST00000643504.2:c.*717_*724delinsGGAAACAT	ENSP00000495157.2:n.*717_*724delinsGGAAACAT
ENST00000646394.1:c.914_921delinsGGAAACAT
ENST00000316562.8:c.1417_1424delinsGGAAACAT	ENSP00000313377.4:p.Gly473=
ENST00000336066.7:c.*428_*435delinsGGAAACAT	ENSP00000477229.1:n.*428_*435delinsGGAAACAT
ENST00000464452.1:n.652_659delinsGGAAACAT
ENST00000495692.5:c.109_116delinsGGAAACAT	ENSP00000476745.1:p.Gly37=
ENST00000497424.5:c.544_551delinsGGAAACAT	ENSP00000417609.1:p.Gly182=
ENST00000610179.5:c.1048_1055delinsGGAAACAT	ENSP00000477429.1:p.Gly350=
ENST00000621507.1:c.544_551delinsGGAAACAT	ENSP00000481523.1:p.Gly182=
NM_024960.4:c.544_551delinsGGAAACAT	NP_079236.3:p.Gly182=
NM_153638.2:c.1417_1424delinsGGAAACAT	NP_705902.2:p.Gly473=
NM_153640.2:c.544_551delinsGGAAACAT	NP_705904.1:p.Gly182=
XM_005260835.2:c.802_809delinsGGAAACAT	XP_005260892.1:p.Gly268=
XM_005260836.3:c.544_551delinsGGAAACAT	XP_005260893.3:p.Gly182=
XM_006723631.1:c.544_551delinsGGAAACAT	XP_006723694.1:p.Gly182=
XM_011529364.1:c.1240_1247delinsGGAAACAT	XP_011527666.1:p.Gly414=
NM_001324191.1:c.544_551delinsGGAAACAT	NP_001311120.1:p.Gly182=
NM_001324193.1:c.109_116delinsGGAAACAT	NP_001311122.1:p.Gly37=
NM_024960.5:c.544_551delinsGGAAACAT	NP_079236.3:p.Gly182=
NM_153638.3:c.1417_1424delinsGGAAACAT	NP_705902.2:p.Gly473=
NM_153640.3:c.544_551delinsGGAAACAT	NP_705904.1:p.Gly182=
NR_136715.1:n.1441_1448delinsGGAAACAT
XM_005260835.3:c.802_809delinsGGAAACAT	XP_005260892.1:p.Gly268=
XM_005260836.4:c.544_551delinsGGAAACAT	XP_005260893.3:p.Gly182=
XM_011529364.3:c.1240_1247delinsGGAAACAT	XP_011527666.1:p.Gly414=
XM_017028077.2:c.109_116delinsGGAAACAT	XP_016883566.1:p.Gly37=
XM_017028078.2:c.109_116delinsGGAAACAT	XP_016883567.1:p.Gly37=
XM_017028079.2:c.109_116delinsGGAAACAT	XP_016883568.1:p.Gly37=
XM_024452002.1:c.109_116delinsGGAAACAT	XP_024307770.1:p.Gly37=
XR_002958533.1:n.2205_2212delinsGGAAACAT
NM_001324191.2:c.544_551delinsGGAAACAT	NP_001311120.1:p.Gly182=
NM_001324193.2:c.109_116delinsGGAAACAT	NP_001311122.1:p.Gly37=
NM_024960.6:c.544_551delinsGGAAACAT	NP_079236.3:p.Gly182=
NR_136715.2:n.988_995delinsGGAAACAT
NM_001386393.1:c.1087_1094delinsGGAAACAT MANE Select	NP_001373322.1:p.Gly363=
NM_153638.4:c.1417_1424delinsGGAAACAT	NP_705902.2:p.Gly473=
NM_153640.4:c.544_551delinsGGAAACAT	NP_705904.1:p.Gly182=