Canonical Allele Identifier: CA408112198

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3907952G>A , CM000682.2:g.3907952G>A	GRCh38
NC_000020.10:g.3888599G>A , CM000682.1:g.3888599G>A	GRCh37
NC_000020.9:g.3836599G>A	NCBI36
NG_008131.3:g.24114G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.325G>A MANE Select	NP_001373322.1:p.Gly109Ser
ENST00000610179.7:c.325G>A MANE Select	ENSP00000477429.2:p.Gly109Ser
NM_001324191.1:c.-219G>A	NP_001311120.1:n.-219G>A
NM_001324191.2:c.-219G>A	NP_001311120.1:n.-219G>A
NM_001324192.1:c.655G>A	NP_001311121.1:p.Gly219Ser
NM_001324193.1:c.-511G>A	NP_001311122.1:n.-511G>A
NM_001324193.2:c.-511G>A	NP_001311122.1:n.-511G>A
NM_024960.4:c.-219G>A	NP_079236.3:n.-219G>A
NM_024960.5:c.-219G>A	NP_079236.3:n.-219G>A
NM_024960.6:c.-219G>A	NP_079236.3:n.-219G>A
NM_153638.2:c.655G>A	NP_705902.2:p.Gly219Ser
NM_153638.3:c.655G>A	NP_705902.2:p.Gly219Ser
NM_153638.4:c.655G>A	NP_705902.2:p.Gly219Ser
NM_153640.2:c.-219G>A	NP_705904.1:n.-219G>A
NM_153640.3:c.-219G>A	NP_705904.1:n.-219G>A
NM_153640.4:c.-219G>A	NP_705904.1:n.-219G>A
NR_136715.1:n.822G>A
NR_136715.2:n.369G>A
ENST00000316562.8:c.655G>A	ENSP00000313377.4:p.Gly219Ser
ENST00000316562.9:c.655G>A	ENSP00000313377.4:p.Gly219Ser
ENST00000336066.7:c.286G>A	ENSP00000477229.1:p.Gly96Ser
ENST00000336066.8:c.325G>A	ENSP00000477229.2:p.Gly109Ser
ENST00000471830.1:n.199G>A
ENST00000495692.5:c.-511G>A	ENSP00000476745.1:n.-511G>A
ENST00000497424.5:c.-219G>A	ENSP00000417609.1:n.-219G>A
ENST00000610179.5:c.286G>A	ENSP00000477429.1:p.Gly96Ser
ENST00000610179.6:c.325G>A	ENSP00000477429.2:p.Gly109Ser
ENST00000621507.1:c.-219G>A	ENSP00000481523.1:n.-219G>A
ENST00000643504.2:c.*98G>A	ENSP00000495157.2:n.*98G>A
ENST00000646394.1:c.152G>A
XM_005260835.2:c.40G>A	XP_005260892.1:p.Gly14Ser
XM_005260835.3:c.40G>A	XP_005260892.1:p.Gly14Ser
XM_005260836.3:c.-219G>A	XP_005260893.3:n.-219G>A
XM_005260836.4:c.-219G>A	XP_005260893.3:n.-219G>A
XM_006723631.1:c.-219G>A	XP_006723694.1:n.-219G>A
XM_011529364.1:c.655G>A	XP_011527666.1:p.Gly219Ser
XM_011529364.3:c.655G>A	XP_011527666.1:p.Gly219Ser
XM_011529365.1:c.655G>A	XP_011527667.1:p.Gly219Ser
XM_011529365.2:c.655G>A	XP_011527667.1:p.Gly219Ser
XM_017028077.2:c.-511G>A	XP_016883566.1:n.-511G>A
XM_017028078.2:c.-511G>A	XP_016883567.1:n.-511G>A
XM_017028079.2:c.-511G>A	XP_016883568.1:n.-511G>A
XM_024452002.1:c.-511G>A	XP_024307770.1:n.-511G>A
XR_002958533.1:n.816G>A