Canonical Allele Identifier: CA2346797861

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912578T= , CM000682.2:g.3912578T=	GRCh38
NC_000020.10:g.3893225T= , CM000682.1:g.3893225T=	GRCh37
NC_000020.9:g.3841225T=	NCBI36
NG_008131.3:g.28740T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1026T= MANE Select	ENSP00000477429.2:p.Asp342=
ENST00000316562.9:c.1356T=	ENSP00000313377.4:p.Asp452=
ENST00000336066.8:c.*367T=	ENSP00000477229.2:n.*367T=
ENST00000610179.6:c.1026T=	ENSP00000477429.2:p.Asp342=
ENST00000643504.2:c.*656T=	ENSP00000495157.2:n.*656T=
ENST00000646394.1:c.853T=
ENST00000316562.8:c.1356T=	ENSP00000313377.4:p.Asp452=
ENST00000336066.7:c.*367T=	ENSP00000477229.1:n.*367T=
ENST00000464452.1:n.591T=
ENST00000495692.5:c.48T=	ENSP00000476745.1:p.Asp16=
ENST00000497424.5:c.483T=	ENSP00000417609.1:p.Asp161=
ENST00000610179.5:c.987T=	ENSP00000477429.1:p.Asp329=
ENST00000621507.1:c.483T=	ENSP00000481523.1:p.Asp161=
NM_024960.4:c.483T=	NP_079236.3:p.Asp161=
NM_153638.2:c.1356T=	NP_705902.2:p.Asp452=
NM_153640.2:c.483T=	NP_705904.1:p.Asp161=
XM_005260835.2:c.741T=	XP_005260892.1:p.Asp247=
XM_005260836.3:c.483T=	XP_005260893.3:p.Asp161=
XM_006723631.1:c.483T=	XP_006723694.1:p.Asp161=
XM_011529364.1:c.1235+1748T=	XP_011527666.1:n.1235+1748T=
NM_001324191.1:c.483T=	NP_001311120.1:p.Asp161=
NM_001324193.1:c.48T=	NP_001311122.1:p.Asp16=
NM_024960.5:c.483T=	NP_079236.3:p.Asp161=
NM_153638.3:c.1356T=	NP_705902.2:p.Asp452=
NM_153640.3:c.483T=	NP_705904.1:p.Asp161=
NR_136715.1:n.1380T=
XM_005260835.3:c.741T=	XP_005260892.1:p.Asp247=
XM_005260836.4:c.483T=	XP_005260893.3:p.Asp161=
XM_011529364.3:c.1235+1748T=	XP_011527666.1:n.1235+1748T=
XM_017028077.2:c.48T=	XP_016883566.1:p.Asp16=
XM_017028078.2:c.48T=	XP_016883567.1:p.Asp16=
XM_017028079.2:c.48T=	XP_016883568.1:p.Asp16=
XM_024452002.1:c.48T=	XP_024307770.1:p.Asp16=
XR_002958533.1:n.2144T=
NM_001324191.2:c.483T=	NP_001311120.1:p.Asp161=
NM_001324193.2:c.48T=	NP_001311122.1:p.Asp16=
NM_024960.6:c.483T=	NP_079236.3:p.Asp161=
NR_136715.2:n.927T=
NM_001386393.1:c.1026T= MANE Select	NP_001373322.1:p.Asp342=
NM_153638.4:c.1356T=	NP_705902.2:p.Asp452=
NM_153640.4:c.483T=	NP_705904.1:p.Asp161=