Canonical Allele Identifier: CA408118027

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3893271G>T (hg19) ; chr20:g.3912624G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912624G>T , CM000682.2:g.3912624G>T	GRCh38
NC_000020.10:g.3893271G>T , CM000682.1:g.3893271G>T	GRCh37
NC_000020.9:g.3841271G>T	NCBI36
NG_008131.3:g.28786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1072G>T MANE Select	ENSP00000477429.2:p.Val358Leu
ENST00000316562.9:c.1402G>T	ENSP00000313377.4:p.Val468Leu
ENST00000336066.8:c.*413G>T	ENSP00000477229.2:n.*413G>T
ENST00000610179.6:c.1072G>T	ENSP00000477429.2:p.Val358Leu
ENST00000643504.2:c.*702G>T	ENSP00000495157.2:n.*702G>T
ENST00000646394.1:c.899G>T
ENST00000316562.8:c.1402G>T	ENSP00000313377.4:p.Val468Leu
ENST00000336066.7:c.*413G>T	ENSP00000477229.1:n.*413G>T
ENST00000464452.1:n.637G>T
ENST00000495692.5:c.94G>T	ENSP00000476745.1:p.Val32Leu
ENST00000497424.5:c.529G>T	ENSP00000417609.1:p.Val177Leu
ENST00000610179.5:c.1033G>T	ENSP00000477429.1:p.Val345Leu
ENST00000621507.1:c.529G>T	ENSP00000481523.1:p.Val177Leu
NM_024960.4:c.529G>T	NP_079236.3:p.Val177Leu
NM_153638.2:c.1402G>T	NP_705902.2:p.Val468Leu
NM_153640.2:c.529G>T	NP_705904.1:p.Val177Leu
XM_005260835.2:c.787G>T	XP_005260892.1:p.Val263Leu
XM_005260836.3:c.529G>T	XP_005260893.3:p.Val177Leu
XM_006723631.1:c.529G>T	XP_006723694.1:p.Val177Leu
XM_011529364.1:c.1235+1794G>T	XP_011527666.1:n.1235+1794G>T
NM_001324191.1:c.529G>T	NP_001311120.1:p.Val177Leu
NM_001324193.1:c.94G>T	NP_001311122.1:p.Val32Leu
NM_024960.5:c.529G>T	NP_079236.3:p.Val177Leu
NM_153638.3:c.1402G>T	NP_705902.2:p.Val468Leu
NM_153640.3:c.529G>T	NP_705904.1:p.Val177Leu
NR_136715.1:n.1426G>T
XM_005260835.3:c.787G>T	XP_005260892.1:p.Val263Leu
XM_005260836.4:c.529G>T	XP_005260893.3:p.Val177Leu
XM_011529364.3:c.1235+1794G>T	XP_011527666.1:n.1235+1794G>T
XM_017028077.2:c.94G>T	XP_016883566.1:p.Val32Leu
XM_017028078.2:c.94G>T	XP_016883567.1:p.Val32Leu
XM_017028079.2:c.94G>T	XP_016883568.1:p.Val32Leu
XM_024452002.1:c.94G>T	XP_024307770.1:p.Val32Leu
XR_002958533.1:n.2190G>T
NM_001324191.2:c.529G>T	NP_001311120.1:p.Val177Leu
NM_001324193.2:c.94G>T	NP_001311122.1:p.Val32Leu
NM_024960.6:c.529G>T	NP_079236.3:p.Val177Leu
NR_136715.2:n.973G>T
NM_001386393.1:c.1072G>T MANE Select	NP_001373322.1:p.Val358Leu
NM_153638.4:c.1402G>T	NP_705902.2:p.Val468Leu
NM_153640.4:c.529G>T	NP_705904.1:p.Val177Leu