Canonical Allele Identifier: CA509423237
Gene: PANK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.3893255A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3912608A>G , CM000682.2:g.3912608A>G GRCh38
NC_000020.10:g.3893255A>G , CM000682.1:g.3893255A>G GRCh37
NC_000020.9:g.3841255A>G NCBI36
NG_008131.3:g.28770A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.1056A>G MANE Select ENSP00000477429.2:p.Gly352=
ENST00000316562.9:c.1386A>G ENSP00000313377.4:p.Gly462=
ENST00000336066.8:c.*397A>G ENSP00000477229.2:n.*397A>G
ENST00000610179.6:c.1056A>G ENSP00000477429.2:p.Gly352=
ENST00000643504.2:c.*686A>G ENSP00000495157.2:n.*686A>G
ENST00000646394.1:c.883A>G
ENST00000316562.8:c.1386A>G ENSP00000313377.4:p.Gly462=
ENST00000336066.7:c.*397A>G ENSP00000477229.1:n.*397A>G
ENST00000464452.1:n.621A>G
ENST00000495692.5:c.78A>G ENSP00000476745.1:p.Gly26=
ENST00000497424.5:c.513A>G ENSP00000417609.1:p.Gly171=
ENST00000610179.5:c.1017A>G ENSP00000477429.1:p.Gly339=
ENST00000621507.1:c.513A>G ENSP00000481523.1:p.Gly171=
NM_024960.4:c.513A>G NP_079236.3:p.Gly171=
NM_153638.2:c.1386A>G NP_705902.2:p.Gly462=
NM_153640.2:c.513A>G NP_705904.1:p.Gly171=
XM_005260835.2:c.771A>G XP_005260892.1:p.Gly257=
XM_005260836.3:c.513A>G XP_005260893.3:p.Gly171=
XM_006723631.1:c.513A>G XP_006723694.1:p.Gly171=
XM_011529364.1:c.1235+1778A>G XP_011527666.1:n.1235+1778A>G
NM_001324191.1:c.513A>G NP_001311120.1:p.Gly171=
NM_001324193.1:c.78A>G NP_001311122.1:p.Gly26=
NM_024960.5:c.513A>G NP_079236.3:p.Gly171=
NM_153638.3:c.1386A>G NP_705902.2:p.Gly462=
NM_153640.3:c.513A>G NP_705904.1:p.Gly171=
NR_136715.1:n.1410A>G
XM_005260835.3:c.771A>G XP_005260892.1:p.Gly257=
XM_005260836.4:c.513A>G XP_005260893.3:p.Gly171=
XM_011529364.3:c.1235+1778A>G XP_011527666.1:n.1235+1778A>G
XM_017028077.2:c.78A>G XP_016883566.1:p.Gly26=
XM_017028078.2:c.78A>G XP_016883567.1:p.Gly26=
XM_017028079.2:c.78A>G XP_016883568.1:p.Gly26=
XM_024452002.1:c.78A>G XP_024307770.1:p.Gly26=
XR_002958533.1:n.2174A>G
NM_001324191.2:c.513A>G NP_001311120.1:p.Gly171=
NM_001324193.2:c.78A>G NP_001311122.1:p.Gly26=
NM_024960.6:c.513A>G NP_079236.3:p.Gly171=
NR_136715.2:n.957A>G
NM_001386393.1:c.1056A>G MANE Select NP_001373322.1:p.Gly352=
NM_153638.4:c.1386A>G NP_705902.2:p.Gly462=
NM_153640.4:c.513A>G NP_705904.1:p.Gly171=