Canonical Allele Identifier: CA509423243

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3893261A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912614A>C , CM000682.2:g.3912614A>C	GRCh38
NC_000020.10:g.3893261A>C , CM000682.1:g.3893261A>C	GRCh37
NC_000020.9:g.3841261A>C	NCBI36
NG_008131.3:g.28776A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1062A>C MANE Select	ENSP00000477429.2:p.Pro354=
ENST00000316562.9:c.1392A>C	ENSP00000313377.4:p.Pro464=
ENST00000336066.8:c.*403A>C	ENSP00000477229.2:n.*403A>C
ENST00000610179.6:c.1062A>C	ENSP00000477429.2:p.Pro354=
ENST00000643504.2:c.*692A>C	ENSP00000495157.2:n.*692A>C
ENST00000646394.1:c.889A>C
ENST00000316562.8:c.1392A>C	ENSP00000313377.4:p.Pro464=
ENST00000336066.7:c.*403A>C	ENSP00000477229.1:n.*403A>C
ENST00000464452.1:n.627A>C
ENST00000495692.5:c.84A>C	ENSP00000476745.1:p.Pro28=
ENST00000497424.5:c.519A>C	ENSP00000417609.1:p.Pro173=
ENST00000610179.5:c.1023A>C	ENSP00000477429.1:p.Pro341=
ENST00000621507.1:c.519A>C	ENSP00000481523.1:p.Pro173=
NM_024960.4:c.519A>C	NP_079236.3:p.Pro173=
NM_153638.2:c.1392A>C	NP_705902.2:p.Pro464=
NM_153640.2:c.519A>C	NP_705904.1:p.Pro173=
XM_005260835.2:c.777A>C	XP_005260892.1:p.Pro259=
XM_005260836.3:c.519A>C	XP_005260893.3:p.Pro173=
XM_006723631.1:c.519A>C	XP_006723694.1:p.Pro173=
XM_011529364.1:c.1235+1784A>C	XP_011527666.1:n.1235+1784A>C
NM_001324191.1:c.519A>C	NP_001311120.1:p.Pro173=
NM_001324193.1:c.84A>C	NP_001311122.1:p.Pro28=
NM_024960.5:c.519A>C	NP_079236.3:p.Pro173=
NM_153638.3:c.1392A>C	NP_705902.2:p.Pro464=
NM_153640.3:c.519A>C	NP_705904.1:p.Pro173=
NR_136715.1:n.1416A>C
XM_005260835.3:c.777A>C	XP_005260892.1:p.Pro259=
XM_005260836.4:c.519A>C	XP_005260893.3:p.Pro173=
XM_011529364.3:c.1235+1784A>C	XP_011527666.1:n.1235+1784A>C
XM_017028077.2:c.84A>C	XP_016883566.1:p.Pro28=
XM_017028078.2:c.84A>C	XP_016883567.1:p.Pro28=
XM_017028079.2:c.84A>C	XP_016883568.1:p.Pro28=
XM_024452002.1:c.84A>C	XP_024307770.1:p.Pro28=
XR_002958533.1:n.2180A>C
NM_001324191.2:c.519A>C	NP_001311120.1:p.Pro173=
NM_001324193.2:c.84A>C	NP_001311122.1:p.Pro28=
NM_024960.6:c.519A>C	NP_079236.3:p.Pro173=
NR_136715.2:n.963A>C
NM_001386393.1:c.1062A>C MANE Select	NP_001373322.1:p.Pro354=
NM_153638.4:c.1392A>C	NP_705902.2:p.Pro464=
NM_153640.4:c.519A>C	NP_705904.1:p.Pro173=