Canonical Allele Identifier: CA408117615

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3893200C>T (hg19) ; chr20:g.3912553C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912553C>T , CM000682.2:g.3912553C>T	GRCh38
NC_000020.10:g.3893200C>T , CM000682.1:g.3893200C>T	GRCh37
NC_000020.9:g.3841200C>T	NCBI36
NG_008131.3:g.28715C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1001C>T MANE Select	ENSP00000477429.2:p.Thr334Ile
ENST00000316562.9:c.1331C>T	ENSP00000313377.4:p.Thr444Ile
ENST00000336066.8:c.*342C>T	ENSP00000477229.2:n.*342C>T
ENST00000610179.6:c.1001C>T	ENSP00000477429.2:p.Thr334Ile
ENST00000643504.2:c.*631C>T	ENSP00000495157.2:n.*631C>T
ENST00000646394.1:c.828C>T
ENST00000316562.8:c.1331C>T	ENSP00000313377.4:p.Thr444Ile
ENST00000336066.7:c.*342C>T	ENSP00000477229.1:n.*342C>T
ENST00000464452.1:n.566C>T
ENST00000495692.5:c.23C>T	ENSP00000476745.1:p.Thr8Ile
ENST00000497424.5:c.458C>T	ENSP00000417609.1:p.Thr153Ile
ENST00000610179.5:c.962C>T	ENSP00000477429.1:p.Thr321Ile
ENST00000621507.1:c.458C>T	ENSP00000481523.1:p.Thr153Ile
NM_024960.4:c.458C>T	NP_079236.3:p.Thr153Ile
NM_153638.2:c.1331C>T	NP_705902.2:p.Thr444Ile
NM_153640.2:c.458C>T	NP_705904.1:p.Thr153Ile
XM_005260835.2:c.716C>T	XP_005260892.1:p.Thr239Ile
XM_005260836.3:c.458C>T	XP_005260893.3:p.Thr153Ile
XM_006723631.1:c.458C>T	XP_006723694.1:p.Thr153Ile
XM_011529364.1:c.1235+1723C>T	XP_011527666.1:n.1235+1723C>T
NM_001324191.1:c.458C>T	NP_001311120.1:p.Thr153Ile
NM_001324193.1:c.23C>T	NP_001311122.1:p.Thr8Ile
NM_024960.5:c.458C>T	NP_079236.3:p.Thr153Ile
NM_153638.3:c.1331C>T	NP_705902.2:p.Thr444Ile
NM_153640.3:c.458C>T	NP_705904.1:p.Thr153Ile
NR_136715.1:n.1355C>T
XM_005260835.3:c.716C>T	XP_005260892.1:p.Thr239Ile
XM_005260836.4:c.458C>T	XP_005260893.3:p.Thr153Ile
XM_011529364.3:c.1235+1723C>T	XP_011527666.1:n.1235+1723C>T
XM_017028077.2:c.23C>T	XP_016883566.1:p.Thr8Ile
XM_017028078.2:c.23C>T	XP_016883567.1:p.Thr8Ile
XM_017028079.2:c.23C>T	XP_016883568.1:p.Thr8Ile
XM_024452002.1:c.23C>T	XP_024307770.1:p.Thr8Ile
XR_002958533.1:n.2119C>T
NM_001324191.2:c.458C>T	NP_001311120.1:p.Thr153Ile
NM_001324193.2:c.23C>T	NP_001311122.1:p.Thr8Ile
NM_024960.6:c.458C>T	NP_079236.3:p.Thr153Ile
NR_136715.2:n.902C>T
NM_001386393.1:c.1001C>T MANE Select	NP_001373322.1:p.Thr334Ile
NM_153638.4:c.1331C>T	NP_705902.2:p.Thr444Ile
NM_153640.4:c.458C>T	NP_705904.1:p.Thr153Ile