Canonical Allele Identifier: CA2346795749
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3908225G= , CM000682.2:g.3908225G= GRCh38
NC_000020.10:g.3888872G= , CM000682.1:g.3888872G= GRCh37
NC_000020.9:g.3836872G= NCBI36
NG_008131.3:g.24387G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610179.7:c.598G= MANE Select ENSP00000477429.2:p.Val200=
ENST00000316562.9:c.928G= ENSP00000313377.4:p.Val310=
ENST00000336066.8:c.508+90G= ENSP00000477229.2:n.508+90G=
ENST00000610179.6:c.598G= ENSP00000477429.2:p.Val200=
ENST00000643504.2:c.*281+90G= ENSP00000495157.2:n.*281+90G=
ENST00000646394.1:c.425G=
ENST00000316562.8:c.928G= ENSP00000313377.4:p.Val310=
ENST00000336066.7:c.469+90G= ENSP00000477229.1:n.469+90G=
ENST00000471830.1:n.382+90G=
ENST00000495692.5:c.-328+90G= ENSP00000476745.1:n.-328+90G=
ENST00000497424.5:c.55G= ENSP00000417609.1:p.Val19=
ENST00000610179.5:c.559G= ENSP00000477429.1:p.Val187=
ENST00000621507.1:c.55G= ENSP00000481523.1:p.Val19=
NM_024960.4:c.55G= NP_079236.3:p.Val19=
NM_153638.2:c.928G= NP_705902.2:p.Val310=
NM_153640.2:c.55G= NP_705904.1:p.Val19=
XM_005260835.2:c.313G= XP_005260892.1:p.Val105=
XM_005260836.3:c.55G= XP_005260893.3:p.Val19=
XM_006723631.1:c.55G= XP_006723694.1:p.Val19=
XM_011529364.1:c.928G= XP_011527666.1:p.Val310=
XM_011529365.1:c.838+90G= XP_011527667.1:n.838+90G=
NM_001324191.1:c.55G= NP_001311120.1:p.Val19=
NM_001324192.1:c.928G= NP_001311121.1:p.Val310=
NM_001324193.1:c.-328+90G= NP_001311122.1:n.-328+90G=
NM_024960.5:c.55G= NP_079236.3:p.Val19=
NM_153638.3:c.928G= NP_705902.2:p.Val310=
NM_153640.3:c.55G= NP_705904.1:p.Val19=
NR_136715.1:n.1005+90G=
XM_005260835.3:c.313G= XP_005260892.1:p.Val105=
XM_005260836.4:c.55G= XP_005260893.3:p.Val19=
XM_011529364.3:c.928G= XP_011527666.1:p.Val310=
XM_011529365.2:c.838+90G= XP_011527667.1:n.838+90G=
XM_017028077.2:c.-328+90G= XP_016883566.1:n.-328+90G=
XM_017028078.2:c.-328+90G= XP_016883567.1:n.-328+90G=
XM_017028079.2:c.-328+90G= XP_016883568.1:n.-328+90G=
XM_024452002.1:c.-328+90G= XP_024307770.1:n.-328+90G=
XR_002958533.1:n.1089G=
NM_001324191.2:c.55G= NP_001311120.1:p.Val19=
NM_001324193.2:c.-328+90G= NP_001311122.1:n.-328+90G=
NM_024960.6:c.55G= NP_079236.3:p.Val19=
NR_136715.2:n.552+90G=
NM_001386393.1:c.598G= MANE Select NP_001373322.1:p.Val200=
NM_153638.4:c.928G= NP_705902.2:p.Val310=
NM_153640.4:c.55G= NP_705904.1:p.Val19=