Canonical Allele Identifier: CA509422740

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3910642T>C , CM000682.2:g.3910642T>C	GRCh38
NC_000020.10:g.3891289T>C , CM000682.1:g.3891289T>C	GRCh37
NC_000020.9:g.3839289T>C	NCBI36
NG_008131.3:g.26804T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001386393.1:c.717T>C MANE Select	NP_001373322.1:p.Ile239=
ENST00000610179.7:c.717T>C MANE Select	ENSP00000477429.2:p.Ile239=
NM_001324191.1:c.174T>C	NP_001311120.1:p.Ile58=
NM_001324191.2:c.174T>C	NP_001311120.1:p.Ile58=
NM_001324193.1:c.-262T>C	NP_001311122.1:n.-262T>C
NM_001324193.2:c.-262T>C	NP_001311122.1:n.-262T>C
NM_024960.4:c.174T>C	NP_079236.3:p.Ile58=
NM_024960.5:c.174T>C	NP_079236.3:p.Ile58=
NM_024960.6:c.174T>C	NP_079236.3:p.Ile58=
NM_153638.2:c.1047T>C	NP_705902.2:p.Ile349=
NM_153638.3:c.1047T>C	NP_705902.2:p.Ile349=
NM_153638.4:c.1047T>C	NP_705902.2:p.Ile349=
NM_153640.2:c.174T>C	NP_705904.1:p.Ile58=
NM_153640.3:c.174T>C	NP_705904.1:p.Ile58=
NM_153640.4:c.174T>C	NP_705904.1:p.Ile58=
NR_136715.1:n.1071T>C
NR_136715.2:n.618T>C
ENST00000316562.8:c.1047T>C	ENSP00000313377.4:p.Ile349=
ENST00000316562.9:c.1047T>C	ENSP00000313377.4:p.Ile349=
ENST00000336066.7:c.*58T>C	ENSP00000477229.1:n.*58T>C
ENST00000336066.8:c.*58T>C	ENSP00000477229.2:n.*58T>C
ENST00000464452.1:n.282T>C
ENST00000471830.1:n.448T>C
ENST00000495692.5:c.-262T>C	ENSP00000476745.1:n.-262T>C
ENST00000497424.5:c.174T>C	ENSP00000417609.1:p.Ile58=
ENST00000610179.5:c.678T>C	ENSP00000477429.1:p.Ile226=
ENST00000610179.6:c.717T>C	ENSP00000477429.2:p.Ile239=
ENST00000621507.1:c.174T>C	ENSP00000481523.1:p.Ile58=
ENST00000643504.2:c.*347T>C	ENSP00000495157.2:n.*347T>C
ENST00000646394.1:c.544T>C
XM_005260835.2:c.432T>C	XP_005260892.1:p.Ile144=
XM_005260835.3:c.432T>C	XP_005260892.1:p.Ile144=
XM_005260836.3:c.174T>C	XP_005260893.3:p.Ile58=
XM_005260836.4:c.174T>C	XP_005260893.3:p.Ile58=
XM_006723631.1:c.174T>C	XP_006723694.1:p.Ile58=
XM_011529364.1:c.1047T>C	XP_011527666.1:p.Ile349=
XM_011529364.3:c.1047T>C	XP_011527666.1:p.Ile349=
XM_017028077.2:c.-262T>C	XP_016883566.1:n.-262T>C
XM_017028078.2:c.-262T>C	XP_016883567.1:n.-262T>C
XM_017028079.2:c.-262T>C	XP_016883568.1:n.-262T>C
XM_024452002.1:c.-262T>C	XP_024307770.1:n.-262T>C
XR_002958533.1:n.1835T>C