Canonical Allele Identifier: CA9750754

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3910619T>C , CM000682.2:g.3910619T>C	GRCh38
NC_000020.10:g.3891266T>C , CM000682.1:g.3891266T>C	GRCh37
NC_000020.9:g.3839266T>C	NCBI36
NG_008131.3:g.26781T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.694T>C MANE Select	NP_001373322.1:p.Leu232=
ENST00000610179.7:c.694T>C MANE Select	ENSP00000477429.2:p.Leu232=
NM_001324191.1:c.151T>C	NP_001311120.1:p.Leu51=
NM_001324191.2:c.151T>C	NP_001311120.1:p.Leu51=
NM_001324193.1:c.-285T>C	NP_001311122.1:n.-285T>C
NM_001324193.2:c.-285T>C	NP_001311122.1:n.-285T>C
NM_024960.4:c.151T>C	NP_079236.3:p.Leu51=
NM_024960.5:c.151T>C	NP_079236.3:p.Leu51=
NM_024960.6:c.151T>C	NP_079236.3:p.Leu51=
NM_153638.2:c.1024T>C	NP_705902.2:p.Leu342=
NM_153638.3:c.1024T>C	NP_705902.2:p.Leu342=
NM_153638.4:c.1024T>C	NP_705902.2:p.Leu342=
NM_153640.2:c.151T>C	NP_705904.1:p.Leu51=
NM_153640.3:c.151T>C	NP_705904.1:p.Leu51=
NM_153640.4:c.151T>C	NP_705904.1:p.Leu51=
NR_136715.1:n.1048T>C
NR_136715.2:n.595T>C
ENST00000316562.8:c.1024T>C	ENSP00000313377.4:p.Leu342=
ENST00000316562.9:c.1024T>C	ENSP00000313377.4:p.Leu342=
ENST00000336066.7:c.*35T>C	ENSP00000477229.1:n.*35T>C
ENST00000336066.8:c.*35T>C	ENSP00000477229.2:n.*35T>C
ENST00000464452.1:n.259T>C
ENST00000471830.1:n.425T>C
ENST00000495692.5:c.-285T>C	ENSP00000476745.1:n.-285T>C
ENST00000497424.5:c.151T>C	ENSP00000417609.1:p.Leu51=
ENST00000610179.5:c.655T>C	ENSP00000477429.1:p.Leu219=
ENST00000610179.6:c.694T>C	ENSP00000477429.2:p.Leu232=
ENST00000621507.1:c.151T>C	ENSP00000481523.1:p.Leu51=
ENST00000643504.2:c.*324T>C	ENSP00000495157.2:n.*324T>C
ENST00000646394.1:c.521T>C
XM_005260835.2:c.409T>C	XP_005260892.1:p.Leu137=
XM_005260835.3:c.409T>C	XP_005260892.1:p.Leu137=
XM_005260836.3:c.151T>C	XP_005260893.3:p.Leu51=
XM_005260836.4:c.151T>C	XP_005260893.3:p.Leu51=
XM_006723631.1:c.151T>C	XP_006723694.1:p.Leu51=
XM_011529364.1:c.1024T>C	XP_011527666.1:p.Leu342=
XM_011529364.3:c.1024T>C	XP_011527666.1:p.Leu342=
XM_017028077.2:c.-285T>C	XP_016883566.1:n.-285T>C
XM_017028078.2:c.-285T>C	XP_016883567.1:n.-285T>C
XM_017028079.2:c.-285T>C	XP_016883568.1:n.-285T>C
XM_024452002.1:c.-285T>C	XP_024307770.1:n.-285T>C
XR_002958533.1:n.1812T>C