Canonical Allele Identifier: CA509423487

Gene: PANK2

Linked Data

• MyVariant Identifiers: chr20:g.3897583C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3916936C>T , CM000682.2:g.3916936C>T	GRCh38
NC_000020.10:g.3897583C>T , CM000682.1:g.3897583C>T	GRCh37
NC_000020.9:g.3845583C>T	NCBI36
NG_008131.3:g.33098C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1092C>T MANE Select	ENSP00000477429.2:p.Asn364=
ENST00000316562.9:c.1422C>T	ENSP00000313377.4:p.Asn474=
ENST00000336066.8:c.*433C>T	ENSP00000477229.2:n.*433C>T
ENST00000610179.6:c.1092C>T	ENSP00000477429.2:p.Asn364=
ENST00000643504.2:c.*722C>T	ENSP00000495157.2:n.*722C>T
ENST00000646394.1:c.919C>T
ENST00000316562.8:c.1422C>T	ENSP00000313377.4:p.Asn474=
ENST00000336066.7:c.*433C>T	ENSP00000477229.1:n.*433C>T
ENST00000464452.1:n.657C>T
ENST00000495692.5:c.114C>T	ENSP00000476745.1:p.Asn38=
ENST00000497424.5:c.549C>T	ENSP00000417609.1:p.Asn183=
ENST00000610179.5:c.1053C>T	ENSP00000477429.1:p.Asn351=
ENST00000621507.1:c.549C>T	ENSP00000481523.1:p.Asn183=
NM_024960.4:c.549C>T	NP_079236.3:p.Asn183=
NM_153638.2:c.1422C>T	NP_705902.2:p.Asn474=
NM_153640.2:c.549C>T	NP_705904.1:p.Asn183=
XM_005260835.2:c.807C>T	XP_005260892.1:p.Asn269=
XM_005260836.3:c.549C>T	XP_005260893.3:p.Asn183=
XM_006723631.1:c.549C>T	XP_006723694.1:p.Asn183=
XM_011529364.1:c.1245C>T	XP_011527666.1:p.Asn415=
NM_001324191.1:c.549C>T	NP_001311120.1:p.Asn183=
NM_001324193.1:c.114C>T	NP_001311122.1:p.Asn38=
NM_024960.5:c.549C>T	NP_079236.3:p.Asn183=
NM_153638.3:c.1422C>T	NP_705902.2:p.Asn474=
NM_153640.3:c.549C>T	NP_705904.1:p.Asn183=
NR_136715.1:n.1446C>T
XM_005260835.3:c.807C>T	XP_005260892.1:p.Asn269=
XM_005260836.4:c.549C>T	XP_005260893.3:p.Asn183=
XM_011529364.3:c.1245C>T	XP_011527666.1:p.Asn415=
XM_017028077.2:c.114C>T	XP_016883566.1:p.Asn38=
XM_017028078.2:c.114C>T	XP_016883567.1:p.Asn38=
XM_017028079.2:c.114C>T	XP_016883568.1:p.Asn38=
XM_024452002.1:c.114C>T	XP_024307770.1:p.Asn38=
XR_002958533.1:n.2210C>T
NM_001324191.2:c.549C>T	NP_001311120.1:p.Asn183=
NM_001324193.2:c.114C>T	NP_001311122.1:p.Asn38=
NM_024960.6:c.549C>T	NP_079236.3:p.Asn183=
NR_136715.2:n.993C>T
NM_001386393.1:c.1092C>T MANE Select	NP_001373322.1:p.Asn364=
NM_153638.4:c.1422C>T	NP_705902.2:p.Asn474=
NM_153640.4:c.549C>T	NP_705904.1:p.Asn183=