Canonical Allele Identifier: CA509422262

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3888649T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3908002T>G , CM000682.2:g.3908002T>G	GRCh38
NC_000020.10:g.3888649T>G , CM000682.1:g.3888649T>G	GRCh37
NC_000020.9:g.3836649T>G	NCBI36
NG_008131.3:g.24164T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000610179.7:c.375T>G MANE Select	ENSP00000477429.2:p.Ala125=
ENST00000316562.9:c.705T>G	ENSP00000313377.4:p.Ala235=
ENST00000336066.8:c.375T>G	ENSP00000477229.2:p.Ala125=
ENST00000610179.6:c.375T>G	ENSP00000477429.2:p.Ala125=
ENST00000643504.2:c.*148T>G	ENSP00000495157.2:n.*148T>G
ENST00000646394.1:c.202T>G
ENST00000316562.8:c.705T>G	ENSP00000313377.4:p.Ala235=
ENST00000336066.7:c.336T>G	ENSP00000477229.1:p.Ala112=
ENST00000471830.1:n.249T>G
ENST00000495692.5:c.-461T>G	ENSP00000476745.1:n.-461T>G
ENST00000497424.5:c.-169T>G	ENSP00000417609.1:n.-169T>G
ENST00000610179.5:c.336T>G	ENSP00000477429.1:p.Ala112=
ENST00000621507.1:c.-169T>G	ENSP00000481523.1:n.-169T>G
NM_024960.4:c.-169T>G	NP_079236.3:n.-169T>G
NM_153638.2:c.705T>G	NP_705902.2:p.Ala235=
NM_153640.2:c.-169T>G	NP_705904.1:n.-169T>G
XM_005260835.2:c.90T>G	XP_005260892.1:p.Ala30=
XM_005260836.3:c.-169T>G	XP_005260893.3:n.-169T>G
XM_006723631.1:c.-169T>G	XP_006723694.1:n.-169T>G
XM_011529364.1:c.705T>G	XP_011527666.1:p.Ala235=
XM_011529365.1:c.705T>G	XP_011527667.1:p.Ala235=
NM_001324191.1:c.-169T>G	NP_001311120.1:n.-169T>G
NM_001324192.1:c.705T>G	NP_001311121.1:p.Ala235=
NM_001324193.1:c.-461T>G	NP_001311122.1:n.-461T>G
NM_024960.5:c.-169T>G	NP_079236.3:n.-169T>G
NM_153638.3:c.705T>G	NP_705902.2:p.Ala235=
NM_153640.3:c.-169T>G	NP_705904.1:n.-169T>G
NR_136715.1:n.872T>G
XM_005260835.3:c.90T>G	XP_005260892.1:p.Ala30=
XM_005260836.4:c.-169T>G	XP_005260893.3:n.-169T>G
XM_011529364.3:c.705T>G	XP_011527666.1:p.Ala235=
XM_011529365.2:c.705T>G	XP_011527667.1:p.Ala235=
XM_017028077.2:c.-461T>G	XP_016883566.1:n.-461T>G
XM_017028078.2:c.-461T>G	XP_016883567.1:n.-461T>G
XM_017028079.2:c.-461T>G	XP_016883568.1:n.-461T>G
XM_024452002.1:c.-461T>G	XP_024307770.1:n.-461T>G
XR_002958533.1:n.866T>G
NM_001324191.2:c.-169T>G	NP_001311120.1:n.-169T>G
NM_001324193.2:c.-461T>G	NP_001311122.1:n.-461T>G
NM_024960.6:c.-169T>G	NP_079236.3:n.-169T>G
NR_136715.2:n.419T>G
NM_001386393.1:c.375T>G MANE Select	NP_001373322.1:p.Ala125=
NM_153638.4:c.705T>G	NP_705902.2:p.Ala235=
NM_153640.4:c.-169T>G	NP_705904.1:n.-169T>G