Canonical Allele Identifier: CA509423138

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3893174T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912527T>A , CM000682.2:g.3912527T>A	GRCh38
NC_000020.10:g.3893174T>A , CM000682.1:g.3893174T>A	GRCh37
NC_000020.9:g.3841174T>A	NCBI36
NG_008131.3:g.28689T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000610179.7:c.975T>A MANE Select	ENSP00000477429.2:p.Leu325=
ENST00000316562.9:c.1305T>A	ENSP00000313377.4:p.Leu435=
ENST00000336066.8:c.*316T>A	ENSP00000477229.2:n.*316T>A
ENST00000610179.6:c.975T>A	ENSP00000477429.2:p.Leu325=
ENST00000643504.2:c.*605T>A	ENSP00000495157.2:n.*605T>A
ENST00000646394.1:c.802T>A
ENST00000316562.8:c.1305T>A	ENSP00000313377.4:p.Leu435=
ENST00000336066.7:c.*316T>A	ENSP00000477229.1:n.*316T>A
ENST00000464452.1:n.540T>A
ENST00000495692.5:c.-4T>A	ENSP00000476745.1:n.-4T>A
ENST00000497424.5:c.432T>A	ENSP00000417609.1:p.Leu144=
ENST00000610179.5:c.936T>A	ENSP00000477429.1:p.Leu312=
ENST00000621507.1:c.432T>A	ENSP00000481523.1:p.Leu144=
NM_024960.4:c.432T>A	NP_079236.3:p.Leu144=
NM_153638.2:c.1305T>A	NP_705902.2:p.Leu435=
NM_153640.2:c.432T>A	NP_705904.1:p.Leu144=
XM_005260835.2:c.690T>A	XP_005260892.1:p.Leu230=
XM_005260836.3:c.432T>A	XP_005260893.3:p.Leu144=
XM_006723631.1:c.432T>A	XP_006723694.1:p.Leu144=
XM_011529364.1:c.1235+1697T>A	XP_011527666.1:n.1235+1697T>A
NM_001324191.1:c.432T>A	NP_001311120.1:p.Leu144=
NM_001324193.1:c.-4T>A	NP_001311122.1:n.-4T>A
NM_024960.5:c.432T>A	NP_079236.3:p.Leu144=
NM_153638.3:c.1305T>A	NP_705902.2:p.Leu435=
NM_153640.3:c.432T>A	NP_705904.1:p.Leu144=
NR_136715.1:n.1329T>A
XM_005260835.3:c.690T>A	XP_005260892.1:p.Leu230=
XM_005260836.4:c.432T>A	XP_005260893.3:p.Leu144=
XM_011529364.3:c.1235+1697T>A	XP_011527666.1:n.1235+1697T>A
XM_017028077.2:c.-4T>A	XP_016883566.1:n.-4T>A
XM_017028078.2:c.-4T>A	XP_016883567.1:n.-4T>A
XM_017028079.2:c.-4T>A	XP_016883568.1:n.-4T>A
XM_024452002.1:c.-4T>A	XP_024307770.1:n.-4T>A
XR_002958533.1:n.2093T>A
NM_001324191.2:c.432T>A	NP_001311120.1:p.Leu144=
NM_001324193.2:c.-4T>A	NP_001311122.1:n.-4T>A
NM_024960.6:c.432T>A	NP_079236.3:p.Leu144=
NR_136715.2:n.876T>A
NM_001386393.1:c.975T>A MANE Select	NP_001373322.1:p.Leu325=
NM_153638.4:c.1305T>A	NP_705902.2:p.Leu435=
NM_153640.4:c.432T>A	NP_705904.1:p.Leu144=