Canonical Allele Identifier: CA408117659

Gene: PANK2

Linked Data

• ClinVar Variation Id: 2627790
• ClinVar RCV Id: RCV003389134
• MyVariant Identifiers: chr20:g.3893208G>T (hg19) ; chr20:g.3912561G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912561G>T , CM000682.2:g.3912561G>T	GRCh38
NC_000020.10:g.3893208G>T , CM000682.1:g.3893208G>T	GRCh37
NC_000020.9:g.3841208G>T	NCBI36
NG_008131.3:g.28723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1009G>T MANE Select	ENSP00000477429.2:p.Asp337Tyr
ENST00000316562.9:c.1339G>T	ENSP00000313377.4:p.Asp447Tyr
ENST00000336066.8:c.*350G>T	ENSP00000477229.2:n.*350G>T
ENST00000610179.6:c.1009G>T	ENSP00000477429.2:p.Asp337Tyr
ENST00000643504.2:c.*639G>T	ENSP00000495157.2:n.*639G>T
ENST00000646394.1:c.836G>T
ENST00000316562.8:c.1339G>T	ENSP00000313377.4:p.Asp447Tyr
ENST00000336066.7:c.*350G>T	ENSP00000477229.1:n.*350G>T
ENST00000464452.1:n.574G>T
ENST00000495692.5:c.31G>T	ENSP00000476745.1:p.Asp11Tyr
ENST00000497424.5:c.466G>T	ENSP00000417609.1:p.Asp156Tyr
ENST00000610179.5:c.970G>T	ENSP00000477429.1:p.Asp324Tyr
ENST00000621507.1:c.466G>T	ENSP00000481523.1:p.Asp156Tyr
NM_024960.4:c.466G>T	NP_079236.3:p.Asp156Tyr
NM_153638.2:c.1339G>T	NP_705902.2:p.Asp447Tyr
NM_153640.2:c.466G>T	NP_705904.1:p.Asp156Tyr
XM_005260835.2:c.724G>T	XP_005260892.1:p.Asp242Tyr
XM_005260836.3:c.466G>T	XP_005260893.3:p.Asp156Tyr
XM_006723631.1:c.466G>T	XP_006723694.1:p.Asp156Tyr
XM_011529364.1:c.1235+1731G>T	XP_011527666.1:n.1235+1731G>T
NM_001324191.1:c.466G>T	NP_001311120.1:p.Asp156Tyr
NM_001324193.1:c.31G>T	NP_001311122.1:p.Asp11Tyr
NM_024960.5:c.466G>T	NP_079236.3:p.Asp156Tyr
NM_153638.3:c.1339G>T	NP_705902.2:p.Asp447Tyr
NM_153640.3:c.466G>T	NP_705904.1:p.Asp156Tyr
NR_136715.1:n.1363G>T
XM_005260835.3:c.724G>T	XP_005260892.1:p.Asp242Tyr
XM_005260836.4:c.466G>T	XP_005260893.3:p.Asp156Tyr
XM_011529364.3:c.1235+1731G>T	XP_011527666.1:n.1235+1731G>T
XM_017028077.2:c.31G>T	XP_016883566.1:p.Asp11Tyr
XM_017028078.2:c.31G>T	XP_016883567.1:p.Asp11Tyr
XM_017028079.2:c.31G>T	XP_016883568.1:p.Asp11Tyr
XM_024452002.1:c.31G>T	XP_024307770.1:p.Asp11Tyr
XR_002958533.1:n.2127G>T
NM_001324191.2:c.466G>T	NP_001311120.1:p.Asp156Tyr
NM_001324193.2:c.31G>T	NP_001311122.1:p.Asp11Tyr
NM_024960.6:c.466G>T	NP_079236.3:p.Asp156Tyr
NR_136715.2:n.910G>T
NM_001386393.1:c.1009G>T MANE Select	NP_001373322.1:p.Asp337Tyr
NM_153638.4:c.1339G>T	NP_705902.2:p.Asp447Tyr
NM_153640.4:c.466G>T	NP_705904.1:p.Asp156Tyr