Canonical Allele Identifier: CA408114379

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3910589C>T , CM000682.2:g.3910589C>T	GRCh38
NC_000020.10:g.3891236C>T , CM000682.1:g.3891236C>T	GRCh37
NC_000020.9:g.3839236C>T	NCBI36
NG_008131.3:g.26751C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.664C>T MANE Select	NP_001373322.1:p.Gln222Ter
ENST00000610179.7:c.664C>T MANE Select	ENSP00000477429.2:p.Gln222Ter
NM_001324191.1:c.121C>T	NP_001311120.1:p.Gln41Ter
NM_001324191.2:c.121C>T	NP_001311120.1:p.Gln41Ter
NM_001324193.1:c.-315C>T	NP_001311122.1:n.-315C>T
NM_001324193.2:c.-315C>T	NP_001311122.1:n.-315C>T
NM_024960.4:c.121C>T	NP_079236.3:p.Gln41Ter
NM_024960.5:c.121C>T	NP_079236.3:p.Gln41Ter
NM_024960.6:c.121C>T	NP_079236.3:p.Gln41Ter
NM_153638.2:c.994C>T	NP_705902.2:p.Gln332Ter
NM_153638.3:c.994C>T	NP_705902.2:p.Gln332Ter
NM_153638.4:c.994C>T	NP_705902.2:p.Gln332Ter
NM_153640.2:c.121C>T	NP_705904.1:p.Gln41Ter
NM_153640.3:c.121C>T	NP_705904.1:p.Gln41Ter
NM_153640.4:c.121C>T	NP_705904.1:p.Gln41Ter
NR_136715.1:n.1018C>T
NR_136715.2:n.565C>T
ENST00000316562.8:c.994C>T	ENSP00000313377.4:p.Gln332Ter
ENST00000316562.9:c.994C>T	ENSP00000313377.4:p.Gln332Ter
ENST00000336066.7:c.*5C>T	ENSP00000477229.1:n.*5C>T
ENST00000336066.8:c.*5C>T	ENSP00000477229.2:n.*5C>T
ENST00000464452.1:n.229C>T
ENST00000471830.1:n.395C>T
ENST00000495692.5:c.-315C>T	ENSP00000476745.1:n.-315C>T
ENST00000497424.5:c.121C>T	ENSP00000417609.1:p.Gln41Ter
ENST00000610179.5:c.625C>T	ENSP00000477429.1:p.Gln209Ter
ENST00000610179.6:c.664C>T	ENSP00000477429.2:p.Gln222Ter
ENST00000621507.1:c.121C>T	ENSP00000481523.1:p.Gln41Ter
ENST00000643504.2:c.*294C>T	ENSP00000495157.2:n.*294C>T
ENST00000646394.1:c.491C>T
XM_005260835.2:c.379C>T	XP_005260892.1:p.Gln127Ter
XM_005260835.3:c.379C>T	XP_005260892.1:p.Gln127Ter
XM_005260836.3:c.121C>T	XP_005260893.3:p.Gln41Ter
XM_005260836.4:c.121C>T	XP_005260893.3:p.Gln41Ter
XM_006723631.1:c.121C>T	XP_006723694.1:p.Gln41Ter
XM_011529364.1:c.994C>T	XP_011527666.1:p.Gln332Ter
XM_011529364.3:c.994C>T	XP_011527666.1:p.Gln332Ter
XM_017028077.2:c.-315C>T	XP_016883566.1:n.-315C>T
XM_017028078.2:c.-315C>T	XP_016883567.1:n.-315C>T
XM_017028079.2:c.-315C>T	XP_016883568.1:n.-315C>T
XM_024452002.1:c.-315C>T	XP_024307770.1:n.-315C>T
XR_002958533.1:n.1782C>T