Canonical Allele Identifier: CA408118041

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3893274G>A (hg19) ; chr20:g.3912627G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912627G>A , CM000682.2:g.3912627G>A	GRCh38
NC_000020.10:g.3893274G>A , CM000682.1:g.3893274G>A	GRCh37
NC_000020.9:g.3841274G>A	NCBI36
NG_008131.3:g.28789G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1075G>A MANE Select	ENSP00000477429.2:p.Ala359Thr
ENST00000316562.9:c.1405G>A	ENSP00000313377.4:p.Ala469Thr
ENST00000336066.8:c.*416G>A	ENSP00000477229.2:n.*416G>A
ENST00000610179.6:c.1075G>A	ENSP00000477429.2:p.Ala359Thr
ENST00000643504.2:c.*705G>A	ENSP00000495157.2:n.*705G>A
ENST00000646394.1:c.902G>A
ENST00000316562.8:c.1405G>A	ENSP00000313377.4:p.Ala469Thr
ENST00000336066.7:c.*416G>A	ENSP00000477229.1:n.*416G>A
ENST00000464452.1:n.640G>A
ENST00000495692.5:c.97G>A	ENSP00000476745.1:p.Ala33Thr
ENST00000497424.5:c.532G>A	ENSP00000417609.1:p.Ala178Thr
ENST00000610179.5:c.1036G>A	ENSP00000477429.1:p.Ala346Thr
ENST00000621507.1:c.532G>A	ENSP00000481523.1:p.Ala178Thr
NM_024960.4:c.532G>A	NP_079236.3:p.Ala178Thr
NM_153638.2:c.1405G>A	NP_705902.2:p.Ala469Thr
NM_153640.2:c.532G>A	NP_705904.1:p.Ala178Thr
XM_005260835.2:c.790G>A	XP_005260892.1:p.Ala264Thr
XM_005260836.3:c.532G>A	XP_005260893.3:p.Ala178Thr
XM_006723631.1:c.532G>A	XP_006723694.1:p.Ala178Thr
XM_011529364.1:c.1235+1797G>A	XP_011527666.1:n.1235+1797G>A
NM_001324191.1:c.532G>A	NP_001311120.1:p.Ala178Thr
NM_001324193.1:c.97G>A	NP_001311122.1:p.Ala33Thr
NM_024960.5:c.532G>A	NP_079236.3:p.Ala178Thr
NM_153638.3:c.1405G>A	NP_705902.2:p.Ala469Thr
NM_153640.3:c.532G>A	NP_705904.1:p.Ala178Thr
NR_136715.1:n.1429G>A
XM_005260835.3:c.790G>A	XP_005260892.1:p.Ala264Thr
XM_005260836.4:c.532G>A	XP_005260893.3:p.Ala178Thr
XM_011529364.3:c.1235+1797G>A	XP_011527666.1:n.1235+1797G>A
XM_017028077.2:c.97G>A	XP_016883566.1:p.Ala33Thr
XM_017028078.2:c.97G>A	XP_016883567.1:p.Ala33Thr
XM_017028079.2:c.97G>A	XP_016883568.1:p.Ala33Thr
XM_024452002.1:c.97G>A	XP_024307770.1:p.Ala33Thr
XR_002958533.1:n.2193G>A
NM_001324191.2:c.532G>A	NP_001311120.1:p.Ala178Thr
NM_001324193.2:c.97G>A	NP_001311122.1:p.Ala33Thr
NM_024960.6:c.532G>A	NP_079236.3:p.Ala178Thr
NR_136715.2:n.976G>A
NM_001386393.1:c.1075G>A MANE Select	NP_001373322.1:p.Ala359Thr
NM_153638.4:c.1405G>A	NP_705902.2:p.Ala469Thr
NM_153640.4:c.532G>A	NP_705904.1:p.Ala178Thr