Canonical Allele Identifier: CA509423486

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3897580A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3916933A>G , CM000682.2:g.3916933A>G	GRCh38
NC_000020.10:g.3897580A>G , CM000682.1:g.3897580A>G	GRCh37
NC_000020.9:g.3845580A>G	NCBI36
NG_008131.3:g.33095A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1089A>G MANE Select	ENSP00000477429.2:p.Gly363=
ENST00000316562.9:c.1419A>G	ENSP00000313377.4:p.Gly473=
ENST00000336066.8:c.*430A>G	ENSP00000477229.2:n.*430A>G
ENST00000610179.6:c.1089A>G	ENSP00000477429.2:p.Gly363=
ENST00000643504.2:c.*719A>G	ENSP00000495157.2:n.*719A>G
ENST00000646394.1:c.916A>G
ENST00000316562.8:c.1419A>G	ENSP00000313377.4:p.Gly473=
ENST00000336066.7:c.*430A>G	ENSP00000477229.1:n.*430A>G
ENST00000464452.1:n.654A>G
ENST00000495692.5:c.111A>G	ENSP00000476745.1:p.Gly37=
ENST00000497424.5:c.546A>G	ENSP00000417609.1:p.Gly182=
ENST00000610179.5:c.1050A>G	ENSP00000477429.1:p.Gly350=
ENST00000621507.1:c.546A>G	ENSP00000481523.1:p.Gly182=
NM_024960.4:c.546A>G	NP_079236.3:p.Gly182=
NM_153638.2:c.1419A>G	NP_705902.2:p.Gly473=
NM_153640.2:c.546A>G	NP_705904.1:p.Gly182=
XM_005260835.2:c.804A>G	XP_005260892.1:p.Gly268=
XM_005260836.3:c.546A>G	XP_005260893.3:p.Gly182=
XM_006723631.1:c.546A>G	XP_006723694.1:p.Gly182=
XM_011529364.1:c.1242A>G	XP_011527666.1:p.Gly414=
NM_001324191.1:c.546A>G	NP_001311120.1:p.Gly182=
NM_001324193.1:c.111A>G	NP_001311122.1:p.Gly37=
NM_024960.5:c.546A>G	NP_079236.3:p.Gly182=
NM_153638.3:c.1419A>G	NP_705902.2:p.Gly473=
NM_153640.3:c.546A>G	NP_705904.1:p.Gly182=
NR_136715.1:n.1443A>G
XM_005260835.3:c.804A>G	XP_005260892.1:p.Gly268=
XM_005260836.4:c.546A>G	XP_005260893.3:p.Gly182=
XM_011529364.3:c.1242A>G	XP_011527666.1:p.Gly414=
XM_017028077.2:c.111A>G	XP_016883566.1:p.Gly37=
XM_017028078.2:c.111A>G	XP_016883567.1:p.Gly37=
XM_017028079.2:c.111A>G	XP_016883568.1:p.Gly37=
XM_024452002.1:c.111A>G	XP_024307770.1:p.Gly37=
XR_002958533.1:n.2207A>G
NM_001324191.2:c.546A>G	NP_001311120.1:p.Gly182=
NM_001324193.2:c.111A>G	NP_001311122.1:p.Gly37=
NM_024960.6:c.546A>G	NP_079236.3:p.Gly182=
NR_136715.2:n.990A>G
NM_001386393.1:c.1089A>G MANE Select	NP_001373322.1:p.Gly363=
NM_153638.4:c.1419A>G	NP_705902.2:p.Gly473=
NM_153640.4:c.546A>G	NP_705904.1:p.Gly182=