Canonical Allele Identifier: CA2346797870

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912601G= , CM000682.2:g.3912601G=	GRCh38
NC_000020.10:g.3893248G= , CM000682.1:g.3893248G=	GRCh37
NC_000020.9:g.3841248G=	NCBI36
NG_008131.3:g.28763G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1049G= MANE Select	ENSP00000477429.2:p.Arg350=
ENST00000316562.9:c.1379G=	ENSP00000313377.4:p.Arg460=
ENST00000336066.8:c.*390G=	ENSP00000477229.2:n.*390G=
ENST00000610179.6:c.1049G=	ENSP00000477429.2:p.Arg350=
ENST00000643504.2:c.*679G=	ENSP00000495157.2:n.*679G=
ENST00000646394.1:c.876G=
ENST00000316562.8:c.1379G=	ENSP00000313377.4:p.Arg460=
ENST00000336066.7:c.*390G=	ENSP00000477229.1:n.*390G=
ENST00000464452.1:n.614G=
ENST00000495692.5:c.71G=	ENSP00000476745.1:p.Arg24=
ENST00000497424.5:c.506G=	ENSP00000417609.1:p.Arg169=
ENST00000610179.5:c.1010G=	ENSP00000477429.1:p.Arg337=
ENST00000621507.1:c.506G=	ENSP00000481523.1:p.Arg169=
NM_024960.4:c.506G=	NP_079236.3:p.Arg169=
NM_153638.2:c.1379G=	NP_705902.2:p.Arg460=
NM_153640.2:c.506G=	NP_705904.1:p.Arg169=
XM_005260835.2:c.764G=	XP_005260892.1:p.Arg255=
XM_005260836.3:c.506G=	XP_005260893.3:p.Arg169=
XM_006723631.1:c.506G=	XP_006723694.1:p.Arg169=
XM_011529364.1:c.1235+1771G=	XP_011527666.1:n.1235+1771G=
NM_001324191.1:c.506G=	NP_001311120.1:p.Arg169=
NM_001324193.1:c.71G=	NP_001311122.1:p.Arg24=
NM_024960.5:c.506G=	NP_079236.3:p.Arg169=
NM_153638.3:c.1379G=	NP_705902.2:p.Arg460=
NM_153640.3:c.506G=	NP_705904.1:p.Arg169=
NR_136715.1:n.1403G=
XM_005260835.3:c.764G=	XP_005260892.1:p.Arg255=
XM_005260836.4:c.506G=	XP_005260893.3:p.Arg169=
XM_011529364.3:c.1235+1771G=	XP_011527666.1:n.1235+1771G=
XM_017028077.2:c.71G=	XP_016883566.1:p.Arg24=
XM_017028078.2:c.71G=	XP_016883567.1:p.Arg24=
XM_017028079.2:c.71G=	XP_016883568.1:p.Arg24=
XM_024452002.1:c.71G=	XP_024307770.1:p.Arg24=
XR_002958533.1:n.2167G=
NM_001324191.2:c.506G=	NP_001311120.1:p.Arg169=
NM_001324193.2:c.71G=	NP_001311122.1:p.Arg24=
NM_024960.6:c.506G=	NP_079236.3:p.Arg169=
NR_136715.2:n.950G=
NM_001386393.1:c.1049G= MANE Select	NP_001373322.1:p.Arg350=
NM_153638.4:c.1379G=	NP_705902.2:p.Arg460=
NM_153640.4:c.506G=	NP_705904.1:p.Arg169=