Canonical Allele Identifier: CA509423257
Gene: PANK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3893279A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912632A>G , CM000682.2:g.3912632A>G GRCh38
NC_000020.10:g.3893279A>G , CM000682.1:g.3893279A>G GRCh37
NC_000020.9:g.3841279A>G NCBI36
NG_008131.3:g.28794A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.1080A>G MANE Select ENSP00000477429.2:p.Ser360=
ENST00000316562.9:c.1410A>G ENSP00000313377.4:p.Ser470=
ENST00000336066.8:c.*421A>G ENSP00000477229.2:n.*421A>G
ENST00000610179.6:c.1080A>G ENSP00000477429.2:p.Ser360=
ENST00000643504.2:c.*710A>G ENSP00000495157.2:n.*710A>G
ENST00000646394.1:c.907A>G
ENST00000316562.8:c.1410A>G ENSP00000313377.4:p.Ser470=
ENST00000336066.7:c.*421A>G ENSP00000477229.1:n.*421A>G
ENST00000464452.1:n.645A>G
ENST00000495692.5:c.102A>G ENSP00000476745.1:p.Ser34=
ENST00000497424.5:c.537A>G ENSP00000417609.1:p.Ser179=
ENST00000610179.5:c.1041A>G ENSP00000477429.1:p.Ser347=
ENST00000621507.1:c.537A>G ENSP00000481523.1:p.Ser179=
NM_024960.4:c.537A>G NP_079236.3:p.Ser179=
NM_153638.2:c.1410A>G NP_705902.2:p.Ser470=
NM_153640.2:c.537A>G NP_705904.1:p.Ser179=
XM_005260835.2:c.795A>G XP_005260892.1:p.Ser265=
XM_005260836.3:c.537A>G XP_005260893.3:p.Ser179=
XM_006723631.1:c.537A>G XP_006723694.1:p.Ser179=
XM_011529364.1:c.1235+1802A>G XP_011527666.1:n.1235+1802A>G
NM_001324191.1:c.537A>G NP_001311120.1:p.Ser179=
NM_001324193.1:c.102A>G NP_001311122.1:p.Ser34=
NM_024960.5:c.537A>G NP_079236.3:p.Ser179=
NM_153638.3:c.1410A>G NP_705902.2:p.Ser470=
NM_153640.3:c.537A>G NP_705904.1:p.Ser179=
NR_136715.1:n.1434A>G
XM_005260835.3:c.795A>G XP_005260892.1:p.Ser265=
XM_005260836.4:c.537A>G XP_005260893.3:p.Ser179=
XM_011529364.3:c.1235+1802A>G XP_011527666.1:n.1235+1802A>G
XM_017028077.2:c.102A>G XP_016883566.1:p.Ser34=
XM_017028078.2:c.102A>G XP_016883567.1:p.Ser34=
XM_017028079.2:c.102A>G XP_016883568.1:p.Ser34=
XM_024452002.1:c.102A>G XP_024307770.1:p.Ser34=
XR_002958533.1:n.2198A>G
NM_001324191.2:c.537A>G NP_001311120.1:p.Ser179=
NM_001324193.2:c.102A>G NP_001311122.1:p.Ser34=
NM_024960.6:c.537A>G NP_079236.3:p.Ser179=
NR_136715.2:n.981A>G
NM_001386393.1:c.1080A>G MANE Select NP_001373322.1:p.Ser360=
NM_153638.4:c.1410A>G NP_705902.2:p.Ser470=
NM_153640.4:c.537A>G NP_705904.1:p.Ser179=