Canonical Allele Identifier: CA408112628

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3908153C>G , CM000682.2:g.3908153C>G	GRCh38
NC_000020.10:g.3888800C>G , CM000682.1:g.3888800C>G	GRCh37
NC_000020.9:g.3836800C>G	NCBI36
NG_008131.3:g.24315C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.526C>G MANE Select	NP_001373322.1:p.Arg176Gly
ENST00000610179.7:c.526C>G MANE Select	ENSP00000477429.2:p.Arg176Gly
NM_001324191.1:c.-18C>G	NP_001311120.1:n.-18C>G
NM_001324191.2:c.-18C>G	NP_001311120.1:n.-18C>G
NM_001324192.1:c.856C>G	NP_001311121.1:p.Arg286Gly
NM_001324193.1:c.-328+18C>G	NP_001311122.1:n.-328+18C>G
NM_001324193.2:c.-328+18C>G	NP_001311122.1:n.-328+18C>G
NM_024960.4:c.-18C>G	NP_079236.3:n.-18C>G
NM_024960.5:c.-18C>G	NP_079236.3:n.-18C>G
NM_024960.6:c.-18C>G	NP_079236.3:n.-18C>G
NM_153638.2:c.856C>G	NP_705902.2:p.Arg286Gly
NM_153638.3:c.856C>G	NP_705902.2:p.Arg286Gly
NM_153638.4:c.856C>G	NP_705902.2:p.Arg286Gly
NM_153640.2:c.-18C>G	NP_705904.1:n.-18C>G
NM_153640.3:c.-18C>G	NP_705904.1:n.-18C>G
NM_153640.4:c.-18C>G	NP_705904.1:n.-18C>G
NR_136715.1:n.1005+18C>G
NR_136715.2:n.552+18C>G
ENST00000316562.8:c.856C>G	ENSP00000313377.4:p.Arg286Gly
ENST00000316562.9:c.856C>G	ENSP00000313377.4:p.Arg286Gly
ENST00000336066.7:c.469+18C>G	ENSP00000477229.1:n.469+18C>G
ENST00000336066.8:c.508+18C>G	ENSP00000477229.2:n.508+18C>G
ENST00000471830.1:n.382+18C>G
ENST00000495692.5:c.-328+18C>G	ENSP00000476745.1:n.-328+18C>G
ENST00000497424.5:c.-18C>G	ENSP00000417609.1:n.-18C>G
ENST00000610179.5:c.487C>G	ENSP00000477429.1:p.Arg163Gly
ENST00000610179.6:c.526C>G	ENSP00000477429.2:p.Arg176Gly
ENST00000621507.1:c.-18C>G	ENSP00000481523.1:n.-18C>G
ENST00000643504.2:c.*281+18C>G	ENSP00000495157.2:n.*281+18C>G
ENST00000646394.1:c.353C>G
XM_005260835.2:c.241C>G	XP_005260892.1:p.Arg81Gly
XM_005260835.3:c.241C>G	XP_005260892.1:p.Arg81Gly
XM_005260836.3:c.-18C>G	XP_005260893.3:n.-18C>G
XM_005260836.4:c.-18C>G	XP_005260893.3:n.-18C>G
XM_006723631.1:c.-18C>G	XP_006723694.1:n.-18C>G
XM_011529364.1:c.856C>G	XP_011527666.1:p.Arg286Gly
XM_011529364.3:c.856C>G	XP_011527666.1:p.Arg286Gly
XM_011529365.1:c.838+18C>G	XP_011527667.1:n.838+18C>G
XM_011529365.2:c.838+18C>G	XP_011527667.1:n.838+18C>G
XM_017028077.2:c.-328+18C>G	XP_016883566.1:n.-328+18C>G
XM_017028078.2:c.-328+18C>G	XP_016883567.1:n.-328+18C>G
XM_017028079.2:c.-328+18C>G	XP_016883568.1:n.-328+18C>G
XM_024452002.1:c.-328+18C>G	XP_024307770.1:n.-328+18C>G
XR_002958533.1:n.1017C>G