Canonical Allele Identifier: CA408117898

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3893250T>A (hg19) ; chr20:g.3912603T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912603T>A , CM000682.2:g.3912603T>A	GRCh38
NC_000020.10:g.3893250T>A , CM000682.1:g.3893250T>A	GRCh37
NC_000020.9:g.3841250T>A	NCBI36
NG_008131.3:g.28765T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1051T>A MANE Select	ENSP00000477429.2:p.Phe351Ile
ENST00000316562.9:c.1381T>A	ENSP00000313377.4:p.Phe461Ile
ENST00000336066.8:c.*392T>A	ENSP00000477229.2:n.*392T>A
ENST00000610179.6:c.1051T>A	ENSP00000477429.2:p.Phe351Ile
ENST00000643504.2:c.*681T>A	ENSP00000495157.2:n.*681T>A
ENST00000646394.1:c.878T>A
ENST00000316562.8:c.1381T>A	ENSP00000313377.4:p.Phe461Ile
ENST00000336066.7:c.*392T>A	ENSP00000477229.1:n.*392T>A
ENST00000464452.1:n.616T>A
ENST00000495692.5:c.73T>A	ENSP00000476745.1:p.Phe25Ile
ENST00000497424.5:c.508T>A	ENSP00000417609.1:p.Phe170Ile
ENST00000610179.5:c.1012T>A	ENSP00000477429.1:p.Phe338Ile
ENST00000621507.1:c.508T>A	ENSP00000481523.1:p.Phe170Ile
NM_024960.4:c.508T>A	NP_079236.3:p.Phe170Ile
NM_153638.2:c.1381T>A	NP_705902.2:p.Phe461Ile
NM_153640.2:c.508T>A	NP_705904.1:p.Phe170Ile
XM_005260835.2:c.766T>A	XP_005260892.1:p.Phe256Ile
XM_005260836.3:c.508T>A	XP_005260893.3:p.Phe170Ile
XM_006723631.1:c.508T>A	XP_006723694.1:p.Phe170Ile
XM_011529364.1:c.1235+1773T>A	XP_011527666.1:n.1235+1773T>A
NM_001324191.1:c.508T>A	NP_001311120.1:p.Phe170Ile
NM_001324193.1:c.73T>A	NP_001311122.1:p.Phe25Ile
NM_024960.5:c.508T>A	NP_079236.3:p.Phe170Ile
NM_153638.3:c.1381T>A	NP_705902.2:p.Phe461Ile
NM_153640.3:c.508T>A	NP_705904.1:p.Phe170Ile
NR_136715.1:n.1405T>A
XM_005260835.3:c.766T>A	XP_005260892.1:p.Phe256Ile
XM_005260836.4:c.508T>A	XP_005260893.3:p.Phe170Ile
XM_011529364.3:c.1235+1773T>A	XP_011527666.1:n.1235+1773T>A
XM_017028077.2:c.73T>A	XP_016883566.1:p.Phe25Ile
XM_017028078.2:c.73T>A	XP_016883567.1:p.Phe25Ile
XM_017028079.2:c.73T>A	XP_016883568.1:p.Phe25Ile
XM_024452002.1:c.73T>A	XP_024307770.1:p.Phe25Ile
XR_002958533.1:n.2169T>A
NM_001324191.2:c.508T>A	NP_001311120.1:p.Phe170Ile
NM_001324193.2:c.73T>A	NP_001311122.1:p.Phe25Ile
NM_024960.6:c.508T>A	NP_079236.3:p.Phe170Ile
NR_136715.2:n.952T>A
NM_001386393.1:c.1051T>A MANE Select	NP_001373322.1:p.Phe351Ile
NM_153638.4:c.1381T>A	NP_705902.2:p.Phe461Ile
NM_153640.4:c.508T>A	NP_705904.1:p.Phe170Ile