Canonical Allele Identifier: CA509422254

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3888646T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3907999T>C , CM000682.2:g.3907999T>C	GRCh38
NC_000020.10:g.3888646T>C , CM000682.1:g.3888646T>C	GRCh37
NC_000020.9:g.3836646T>C	NCBI36
NG_008131.3:g.24161T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000610179.7:c.372T>C MANE Select	ENSP00000477429.2:p.Thr124=
ENST00000316562.9:c.702T>C	ENSP00000313377.4:p.Thr234=
ENST00000336066.8:c.372T>C	ENSP00000477229.2:p.Thr124=
ENST00000610179.6:c.372T>C	ENSP00000477429.2:p.Thr124=
ENST00000643504.2:c.*145T>C	ENSP00000495157.2:n.*145T>C
ENST00000646394.1:c.199T>C
ENST00000316562.8:c.702T>C	ENSP00000313377.4:p.Thr234=
ENST00000336066.7:c.333T>C	ENSP00000477229.1:p.Thr111=
ENST00000471830.1:n.246T>C
ENST00000495692.5:c.-464T>C	ENSP00000476745.1:n.-464T>C
ENST00000497424.5:c.-172T>C	ENSP00000417609.1:n.-172T>C
ENST00000610179.5:c.333T>C	ENSP00000477429.1:p.Thr111=
ENST00000621507.1:c.-172T>C	ENSP00000481523.1:n.-172T>C
NM_024960.4:c.-172T>C	NP_079236.3:n.-172T>C
NM_153638.2:c.702T>C	NP_705902.2:p.Thr234=
NM_153640.2:c.-172T>C	NP_705904.1:n.-172T>C
XM_005260835.2:c.87T>C	XP_005260892.1:p.Thr29=
XM_005260836.3:c.-172T>C	XP_005260893.3:n.-172T>C
XM_006723631.1:c.-172T>C	XP_006723694.1:n.-172T>C
XM_011529364.1:c.702T>C	XP_011527666.1:p.Thr234=
XM_011529365.1:c.702T>C	XP_011527667.1:p.Thr234=
NM_001324191.1:c.-172T>C	NP_001311120.1:n.-172T>C
NM_001324192.1:c.702T>C	NP_001311121.1:p.Thr234=
NM_001324193.1:c.-464T>C	NP_001311122.1:n.-464T>C
NM_024960.5:c.-172T>C	NP_079236.3:n.-172T>C
NM_153638.3:c.702T>C	NP_705902.2:p.Thr234=
NM_153640.3:c.-172T>C	NP_705904.1:n.-172T>C
NR_136715.1:n.869T>C
XM_005260835.3:c.87T>C	XP_005260892.1:p.Thr29=
XM_005260836.4:c.-172T>C	XP_005260893.3:n.-172T>C
XM_011529364.3:c.702T>C	XP_011527666.1:p.Thr234=
XM_011529365.2:c.702T>C	XP_011527667.1:p.Thr234=
XM_017028077.2:c.-464T>C	XP_016883566.1:n.-464T>C
XM_017028078.2:c.-464T>C	XP_016883567.1:n.-464T>C
XM_017028079.2:c.-464T>C	XP_016883568.1:n.-464T>C
XM_024452002.1:c.-464T>C	XP_024307770.1:n.-464T>C
XR_002958533.1:n.863T>C
NM_001324191.2:c.-172T>C	NP_001311120.1:n.-172T>C
NM_001324193.2:c.-464T>C	NP_001311122.1:n.-464T>C
NM_024960.6:c.-172T>C	NP_079236.3:n.-172T>C
NR_136715.2:n.416T>C
NM_001386393.1:c.372T>C MANE Select	NP_001373322.1:p.Thr124=
NM_153638.4:c.702T>C	NP_705902.2:p.Thr234=
NM_153640.4:c.-172T>C	NP_705904.1:n.-172T>C