Canonical Allele Identifier: CA509423483

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3897577T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3916930T>C , CM000682.2:g.3916930T>C	GRCh38
NC_000020.10:g.3897577T>C , CM000682.1:g.3897577T>C	GRCh37
NC_000020.9:g.3845577T>C	NCBI36
NG_008131.3:g.33092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1086T>C MANE Select	ENSP00000477429.2:p.Phe362=
ENST00000316562.9:c.1416T>C	ENSP00000313377.4:p.Phe472=
ENST00000336066.8:c.*427T>C	ENSP00000477229.2:n.*427T>C
ENST00000610179.6:c.1086T>C	ENSP00000477429.2:p.Phe362=
ENST00000643504.2:c.*716T>C	ENSP00000495157.2:n.*716T>C
ENST00000646394.1:c.913T>C
ENST00000316562.8:c.1416T>C	ENSP00000313377.4:p.Phe472=
ENST00000336066.7:c.*427T>C	ENSP00000477229.1:n.*427T>C
ENST00000464452.1:n.651T>C
ENST00000495692.5:c.108T>C	ENSP00000476745.1:p.Phe36=
ENST00000497424.5:c.543T>C	ENSP00000417609.1:p.Phe181=
ENST00000610179.5:c.1047T>C	ENSP00000477429.1:p.Phe349=
ENST00000621507.1:c.543T>C	ENSP00000481523.1:p.Phe181=
NM_024960.4:c.543T>C	NP_079236.3:p.Phe181=
NM_153638.2:c.1416T>C	NP_705902.2:p.Phe472=
NM_153640.2:c.543T>C	NP_705904.1:p.Phe181=
XM_005260835.2:c.801T>C	XP_005260892.1:p.Phe267=
XM_005260836.3:c.543T>C	XP_005260893.3:p.Phe181=
XM_006723631.1:c.543T>C	XP_006723694.1:p.Phe181=
XM_011529364.1:c.1239T>C	XP_011527666.1:p.Phe413=
NM_001324191.1:c.543T>C	NP_001311120.1:p.Phe181=
NM_001324193.1:c.108T>C	NP_001311122.1:p.Phe36=
NM_024960.5:c.543T>C	NP_079236.3:p.Phe181=
NM_153638.3:c.1416T>C	NP_705902.2:p.Phe472=
NM_153640.3:c.543T>C	NP_705904.1:p.Phe181=
NR_136715.1:n.1440T>C
XM_005260835.3:c.801T>C	XP_005260892.1:p.Phe267=
XM_005260836.4:c.543T>C	XP_005260893.3:p.Phe181=
XM_011529364.3:c.1239T>C	XP_011527666.1:p.Phe413=
XM_017028077.2:c.108T>C	XP_016883566.1:p.Phe36=
XM_017028078.2:c.108T>C	XP_016883567.1:p.Phe36=
XM_017028079.2:c.108T>C	XP_016883568.1:p.Phe36=
XM_024452002.1:c.108T>C	XP_024307770.1:p.Phe36=
XR_002958533.1:n.2204T>C
NM_001324191.2:c.543T>C	NP_001311120.1:p.Phe181=
NM_001324193.2:c.108T>C	NP_001311122.1:p.Phe36=
NM_024960.6:c.543T>C	NP_079236.3:p.Phe181=
NR_136715.2:n.987T>C
NM_001386393.1:c.1086T>C MANE Select	NP_001373322.1:p.Phe362=
NM_153638.4:c.1416T>C	NP_705902.2:p.Phe472=
NM_153640.4:c.543T>C	NP_705904.1:p.Phe181=