Canonical Allele Identifier: CA408119528

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3917040C>T , CM000682.2:g.3917040C>T	GRCh38
NC_000020.10:g.3897687C>T , CM000682.1:g.3897687C>T	GRCh37
NC_000020.9:g.3845687C>T	NCBI36
NG_008131.3:g.33202C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.1196C>T MANE Select	NP_001373322.1:p.Ala399Val
ENST00000610179.7:c.1196C>T MANE Select	ENSP00000477429.2:p.Ala399Val
NM_001324191.1:c.653C>T	NP_001311120.1:p.Ala218Val
NM_001324191.2:c.653C>T	NP_001311120.1:p.Ala218Val
NM_001324193.1:c.218C>T	NP_001311122.1:p.Ala73Val
NM_001324193.2:c.218C>T	NP_001311122.1:p.Ala73Val
NM_024960.4:c.653C>T	NP_079236.3:p.Ala218Val
NM_024960.5:c.653C>T	NP_079236.3:p.Ala218Val
NM_024960.6:c.653C>T	NP_079236.3:p.Ala218Val
NM_153638.2:c.1526C>T	NP_705902.2:p.Ala509Val
NM_153638.3:c.1526C>T	NP_705902.2:p.Ala509Val
NM_153638.4:c.1526C>T	NP_705902.2:p.Ala509Val
NM_153640.2:c.653C>T	NP_705904.1:p.Ala218Val
NM_153640.3:c.653C>T	NP_705904.1:p.Ala218Val
NM_153640.4:c.653C>T	NP_705904.1:p.Ala218Val
NR_136715.1:n.1550C>T
NR_136715.2:n.1097C>T
ENST00000316562.8:c.1526C>T	ENSP00000313377.4:p.Ala509Val
ENST00000316562.9:c.1526C>T	ENSP00000313377.4:p.Ala509Val
ENST00000336066.7:c.*537C>T	ENSP00000477229.1:n.*537C>T
ENST00000336066.8:c.*537C>T	ENSP00000477229.2:n.*537C>T
ENST00000464452.1:n.761C>T
ENST00000495692.5:c.218C>T	ENSP00000476745.1:p.Ala73Val
ENST00000497424.5:c.653C>T	ENSP00000417609.1:p.Ala218Val
ENST00000610179.5:c.1157C>T	ENSP00000477429.1:p.Ala386Val
ENST00000610179.6:c.1196C>T	ENSP00000477429.2:p.Ala399Val
ENST00000621507.1:c.653C>T	ENSP00000481523.1:p.Ala218Val
ENST00000643504.2:c.*826C>T	ENSP00000495157.2:n.*826C>T
ENST00000646394.1:c.1023C>T
XM_005260835.2:c.911C>T	XP_005260892.1:p.Ala304Val
XM_005260835.3:c.911C>T	XP_005260892.1:p.Ala304Val
XM_005260836.3:c.653C>T	XP_005260893.3:p.Ala218Val
XM_005260836.4:c.653C>T	XP_005260893.3:p.Ala218Val
XM_006723631.1:c.653C>T	XP_006723694.1:p.Ala218Val
XM_011529364.1:c.1349C>T	XP_011527666.1:p.Ala450Val
XM_011529364.3:c.1349C>T	XP_011527666.1:p.Ala450Val
XM_017028077.2:c.218C>T	XP_016883566.1:p.Ala73Val
XM_017028078.2:c.218C>T	XP_016883567.1:p.Ala73Val
XM_017028079.2:c.218C>T	XP_016883568.1:p.Ala73Val
XM_024452002.1:c.218C>T	XP_024307770.1:p.Ala73Val
XR_002958533.1:n.2314C>T