Canonical Allele Identifier: CA408112316

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3888653G>T (hg19) ; chr20:g.3908006G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3908006G>T , CM000682.2:g.3908006G>T	GRCh38
NC_000020.10:g.3888653G>T , CM000682.1:g.3888653G>T	GRCh37
NC_000020.9:g.3836653G>T	NCBI36
NG_008131.3:g.24168G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000610179.7:c.379G>T MANE Select	ENSP00000477429.2:p.Glu127Ter
ENST00000316562.9:c.709G>T	ENSP00000313377.4:p.Glu237Ter
ENST00000336066.8:c.379G>T	ENSP00000477229.2:p.Glu127Ter
ENST00000610179.6:c.379G>T	ENSP00000477429.2:p.Glu127Ter
ENST00000643504.2:c.*152G>T	ENSP00000495157.2:n.*152G>T
ENST00000646394.1:c.206G>T
ENST00000316562.8:c.709G>T	ENSP00000313377.4:p.Glu237Ter
ENST00000336066.7:c.340G>T	ENSP00000477229.1:p.Glu114Ter
ENST00000471830.1:n.253G>T
ENST00000495692.5:c.-457G>T	ENSP00000476745.1:n.-457G>T
ENST00000497424.5:c.-165G>T	ENSP00000417609.1:n.-165G>T
ENST00000610179.5:c.340G>T	ENSP00000477429.1:p.Glu114Ter
ENST00000621507.1:c.-165G>T	ENSP00000481523.1:n.-165G>T
NM_024960.4:c.-165G>T	NP_079236.3:n.-165G>T
NM_153638.2:c.709G>T	NP_705902.2:p.Glu237Ter
NM_153640.2:c.-165G>T	NP_705904.1:n.-165G>T
XM_005260835.2:c.94G>T	XP_005260892.1:p.Glu32Ter
XM_005260836.3:c.-165G>T	XP_005260893.3:n.-165G>T
XM_006723631.1:c.-165G>T	XP_006723694.1:n.-165G>T
XM_011529364.1:c.709G>T	XP_011527666.1:p.Glu237Ter
XM_011529365.1:c.709G>T	XP_011527667.1:p.Glu237Ter
NM_001324191.1:c.-165G>T	NP_001311120.1:n.-165G>T
NM_001324192.1:c.709G>T	NP_001311121.1:p.Glu237Ter
NM_001324193.1:c.-457G>T	NP_001311122.1:n.-457G>T
NM_024960.5:c.-165G>T	NP_079236.3:n.-165G>T
NM_153638.3:c.709G>T	NP_705902.2:p.Glu237Ter
NM_153640.3:c.-165G>T	NP_705904.1:n.-165G>T
NR_136715.1:n.876G>T
XM_005260835.3:c.94G>T	XP_005260892.1:p.Glu32Ter
XM_005260836.4:c.-165G>T	XP_005260893.3:n.-165G>T
XM_011529364.3:c.709G>T	XP_011527666.1:p.Glu237Ter
XM_011529365.2:c.709G>T	XP_011527667.1:p.Glu237Ter
XM_017028077.2:c.-457G>T	XP_016883566.1:n.-457G>T
XM_017028078.2:c.-457G>T	XP_016883567.1:n.-457G>T
XM_017028079.2:c.-457G>T	XP_016883568.1:n.-457G>T
XM_024452002.1:c.-457G>T	XP_024307770.1:n.-457G>T
XR_002958533.1:n.870G>T
NM_001324191.2:c.-165G>T	NP_001311120.1:n.-165G>T
NM_001324193.2:c.-457G>T	NP_001311122.1:n.-457G>T
NM_024960.6:c.-165G>T	NP_079236.3:n.-165G>T
NR_136715.2:n.423G>T
NM_001386393.1:c.379G>T MANE Select	NP_001373322.1:p.Glu127Ter
NM_153638.4:c.709G>T	NP_705902.2:p.Glu237Ter
NM_153640.4:c.-165G>T	NP_705904.1:n.-165G>T