Canonical Allele Identifier: CA9750820

Gene: PANK2

Linked Data

• dbSNP Id: rs775905898
• ExAC: 20:3893212 A / G
• gnomAD v2: 20-3893212-A-G
• gnomAD v4: 20-3912565-A-G
• MyVariant Identifiers: chr20:g.3893212A>G (hg19) ; chr20:g.3912565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912565A>G , CM000682.2:g.3912565A>G	GRCh38
NC_000020.10:g.3893212A>G , CM000682.1:g.3893212A>G	GRCh37
NC_000020.9:g.3841212A>G	NCBI36
NG_008131.3:g.28727A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1013A>G MANE Select	ENSP00000477429.2:p.Lys338Arg
ENST00000316562.9:c.1343A>G	ENSP00000313377.4:p.Lys448Arg
ENST00000336066.8:c.*354A>G	ENSP00000477229.2:n.*354A>G
ENST00000610179.6:c.1013A>G	ENSP00000477429.2:p.Lys338Arg
ENST00000643504.2:c.*643A>G	ENSP00000495157.2:n.*643A>G
ENST00000646394.1:c.840A>G
ENST00000316562.8:c.1343A>G	ENSP00000313377.4:p.Lys448Arg
ENST00000336066.7:c.*354A>G	ENSP00000477229.1:n.*354A>G
ENST00000464452.1:n.578A>G
ENST00000495692.5:c.35A>G	ENSP00000476745.1:p.Lys12Arg
ENST00000497424.5:c.470A>G	ENSP00000417609.1:p.Lys157Arg
ENST00000610179.5:c.974A>G	ENSP00000477429.1:p.Lys325Arg
ENST00000621507.1:c.470A>G	ENSP00000481523.1:p.Lys157Arg
NM_024960.4:c.470A>G	NP_079236.3:p.Lys157Arg
NM_153638.2:c.1343A>G	NP_705902.2:p.Lys448Arg
NM_153640.2:c.470A>G	NP_705904.1:p.Lys157Arg
XM_005260835.2:c.728A>G	XP_005260892.1:p.Lys243Arg
XM_005260836.3:c.470A>G	XP_005260893.3:p.Lys157Arg
XM_006723631.1:c.470A>G	XP_006723694.1:p.Lys157Arg
XM_011529364.1:c.1235+1735A>G	XP_011527666.1:n.1235+1735A>G
NM_001324191.1:c.470A>G	NP_001311120.1:p.Lys157Arg
NM_001324193.1:c.35A>G	NP_001311122.1:p.Lys12Arg
NM_024960.5:c.470A>G	NP_079236.3:p.Lys157Arg
NM_153638.3:c.1343A>G	NP_705902.2:p.Lys448Arg
NM_153640.3:c.470A>G	NP_705904.1:p.Lys157Arg
NR_136715.1:n.1367A>G
XM_005260835.3:c.728A>G	XP_005260892.1:p.Lys243Arg
XM_005260836.4:c.470A>G	XP_005260893.3:p.Lys157Arg
XM_011529364.3:c.1235+1735A>G	XP_011527666.1:n.1235+1735A>G
XM_017028077.2:c.35A>G	XP_016883566.1:p.Lys12Arg
XM_017028078.2:c.35A>G	XP_016883567.1:p.Lys12Arg
XM_017028079.2:c.35A>G	XP_016883568.1:p.Lys12Arg
XM_024452002.1:c.35A>G	XP_024307770.1:p.Lys12Arg
XR_002958533.1:n.2131A>G
NM_001324191.2:c.470A>G	NP_001311120.1:p.Lys157Arg
NM_001324193.2:c.35A>G	NP_001311122.1:p.Lys12Arg
NM_024960.6:c.470A>G	NP_079236.3:p.Lys157Arg
NR_136715.2:n.914A>G
NM_001386393.1:c.1013A>G MANE Select	NP_001373322.1:p.Lys338Arg
NM_153638.4:c.1343A>G	NP_705902.2:p.Lys448Arg
NM_153640.4:c.470A>G	NP_705904.1:p.Lys157Arg