Canonical Allele Identifier: CA408112118

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3907935G>A , CM000682.2:g.3907935G>A	GRCh38
NC_000020.10:g.3888582G>A , CM000682.1:g.3888582G>A	GRCh37
NC_000020.9:g.3836582G>A	NCBI36
NG_008131.3:g.24097G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.308G>A MANE Select	NP_001373322.1:p.Trp103Ter
ENST00000610179.7:c.308G>A MANE Select	ENSP00000477429.2:p.Trp103Ter
NM_001324191.1:c.-236G>A	NP_001311120.1:n.-236G>A
NM_001324191.2:c.-236G>A	NP_001311120.1:n.-236G>A
NM_001324192.1:c.638G>A	NP_001311121.1:p.Trp213Ter
NM_001324193.1:c.-528G>A	NP_001311122.1:n.-528G>A
NM_001324193.2:c.-528G>A	NP_001311122.1:n.-528G>A
NM_024960.4:c.-236G>A	NP_079236.3:n.-236G>A
NM_024960.5:c.-236G>A	NP_079236.3:n.-236G>A
NM_024960.6:c.-236G>A	NP_079236.3:n.-236G>A
NM_153638.2:c.638G>A	NP_705902.2:p.Trp213Ter
NM_153638.3:c.638G>A	NP_705902.2:p.Trp213Ter
NM_153638.4:c.638G>A	NP_705902.2:p.Trp213Ter
NM_153640.2:c.-236G>A	NP_705904.1:n.-236G>A
NM_153640.3:c.-236G>A	NP_705904.1:n.-236G>A
NM_153640.4:c.-236G>A	NP_705904.1:n.-236G>A
NR_136715.1:n.805G>A
NR_136715.2:n.352G>A
ENST00000316562.8:c.638G>A	ENSP00000313377.4:p.Trp213Ter
ENST00000316562.9:c.638G>A	ENSP00000313377.4:p.Trp213Ter
ENST00000336066.7:c.269G>A	ENSP00000477229.1:p.Trp90Ter
ENST00000336066.8:c.308G>A	ENSP00000477229.2:p.Trp103Ter
ENST00000471830.1:n.182G>A
ENST00000495692.5:c.-528G>A	ENSP00000476745.1:n.-528G>A
ENST00000497424.5:c.-236G>A	ENSP00000417609.1:n.-236G>A
ENST00000610179.5:c.269G>A	ENSP00000477429.1:p.Trp90Ter
ENST00000610179.6:c.308G>A	ENSP00000477429.2:p.Trp103Ter
ENST00000621507.1:c.-236G>A	ENSP00000481523.1:n.-236G>A
ENST00000643504.2:c.*81G>A	ENSP00000495157.2:n.*81G>A
ENST00000646394.1:c.135G>A
XM_005260835.2:c.23G>A	XP_005260892.1:p.Trp8Ter
XM_005260835.3:c.23G>A	XP_005260892.1:p.Trp8Ter
XM_005260836.3:c.-236G>A	XP_005260893.3:n.-236G>A
XM_005260836.4:c.-236G>A	XP_005260893.3:n.-236G>A
XM_006723631.1:c.-236G>A	XP_006723694.1:n.-236G>A
XM_011529364.1:c.638G>A	XP_011527666.1:p.Trp213Ter
XM_011529364.3:c.638G>A	XP_011527666.1:p.Trp213Ter
XM_011529365.1:c.638G>A	XP_011527667.1:p.Trp213Ter
XM_011529365.2:c.638G>A	XP_011527667.1:p.Trp213Ter
XM_017028077.2:c.-528G>A	XP_016883566.1:n.-528G>A
XM_017028078.2:c.-528G>A	XP_016883567.1:n.-528G>A
XM_017028079.2:c.-528G>A	XP_016883568.1:n.-528G>A
XM_024452002.1:c.-528G>A	XP_024307770.1:n.-528G>A
XR_002958533.1:n.799G>A