Canonical Allele Identifier: CA2346795614

Gene: PANK2

Linked Data

• dbSNP Id: rs2090412149

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3907912_3907913insTC , CM000682.2:g.3907912_3907913insTC	GRCh38
NC_000020.10:g.3888559_3888560insTC , CM000682.1:g.3888559_3888560insTC	GRCh37
NC_000020.9:g.3836559_3836560insTC	NCBI36
NG_008131.3:g.24074_24075insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000610179.7:c.299-14_299-13insTC MANE Select	ENSP00000477429.2:n.299-14_299-13insTC
ENST00000316562.9:c.629-14_629-13insTC	ENSP00000313377.4:n.629-14_629-13insTC
ENST00000336066.8:c.299-14_299-13insTC	ENSP00000477229.2:n.299-14_299-13insTC
ENST00000610179.6:c.299-14_299-13insTC	ENSP00000477429.2:n.299-14_299-13insTC
ENST00000643504.2:c.*72-14_*72-13insTC	ENSP00000495157.2:n.*72-14_*72-13insTC
ENST00000646394.1:c.126-14_126-13insTC
ENST00000316562.8:c.629-14_629-13insTC	ENSP00000313377.4:n.629-14_629-13insTC
ENST00000336066.7:c.260-14_260-13insTC	ENSP00000477229.1:n.260-14_260-13insTC
ENST00000471830.1:n.173-14_173-13insTC
ENST00000495692.5:c.-537-14_-537-13insTC	ENSP00000476745.1:n.-537-14_-537-13insTC
ENST00000497424.5:c.-245-14_-245-13insTC	ENSP00000417609.1:n.-245-14_-245-13insTC
ENST00000610179.5:c.260-14_260-13insTC	ENSP00000477429.1:n.260-14_260-13insTC
ENST00000621507.1:c.-245-14_-245-13insTC	ENSP00000481523.1:n.-245-14_-245-13insTC
NM_024960.4:c.-245-14_-245-13insTC	NP_079236.3:n.-245-14_-245-13insTC
NM_153638.2:c.629-14_629-13insTC	NP_705902.2:n.629-14_629-13insTC
NM_153640.2:c.-245-14_-245-13insTC	NP_705904.1:n.-245-14_-245-13insTC
XM_005260835.2:c.14-14_14-13insTC	XP_005260892.1:n.14-14_14-13insTC
XM_005260836.3:c.-245-14_-245-13insTC	XP_005260893.3:n.-245-14_-245-13insTC
XM_006723631.1:c.-245-14_-245-13insTC	XP_006723694.1:n.-245-14_-245-13insTC
XM_011529364.1:c.629-14_629-13insTC	XP_011527666.1:n.629-14_629-13insTC
XM_011529365.1:c.629-14_629-13insTC	XP_011527667.1:n.629-14_629-13insTC
NM_001324191.1:c.-245-14_-245-13insTC	NP_001311120.1:n.-245-14_-245-13insTC
NM_001324192.1:c.629-14_629-13insTC	NP_001311121.1:n.629-14_629-13insTC
NM_001324193.1:c.-537-14_-537-13insTC	NP_001311122.1:n.-537-14_-537-13insTC
NM_024960.5:c.-245-14_-245-13insTC	NP_079236.3:n.-245-14_-245-13insTC
NM_153638.3:c.629-14_629-13insTC	NP_705902.2:n.629-14_629-13insTC
NM_153640.3:c.-245-14_-245-13insTC	NP_705904.1:n.-245-14_-245-13insTC
NR_136715.1:n.796-14_796-13insTC
XM_005260835.3:c.14-14_14-13insTC	XP_005260892.1:n.14-14_14-13insTC
XM_005260836.4:c.-245-14_-245-13insTC	XP_005260893.3:n.-245-14_-245-13insTC
XM_011529364.3:c.629-14_629-13insTC	XP_011527666.1:n.629-14_629-13insTC
XM_011529365.2:c.629-14_629-13insTC	XP_011527667.1:n.629-14_629-13insTC
XM_017028077.2:c.-537-14_-537-13insTC	XP_016883566.1:n.-537-14_-537-13insTC
XM_017028078.2:c.-537-14_-537-13insTC	XP_016883567.1:n.-537-14_-537-13insTC
XM_017028079.2:c.-537-14_-537-13insTC	XP_016883568.1:n.-537-14_-537-13insTC
XM_024452002.1:c.-537-14_-537-13insTC	XP_024307770.1:n.-537-14_-537-13insTC
XR_002958533.1:n.790-14_790-13insTC
NM_001324191.2:c.-245-14_-245-13insTC	NP_001311120.1:n.-245-14_-245-13insTC
NM_001324193.2:c.-537-14_-537-13insTC	NP_001311122.1:n.-537-14_-537-13insTC
NM_024960.6:c.-245-14_-245-13insTC	NP_079236.3:n.-245-14_-245-13insTC
NR_136715.2:n.343-14_343-13insTC
NM_001386393.1:c.299-14_299-13insTC MANE Select	NP_001373322.1:n.299-14_299-13insTC
NM_153638.4:c.629-14_629-13insTC	NP_705902.2:n.629-14_629-13insTC
NM_153640.4:c.-245-14_-245-13insTC	NP_705904.1:n.-245-14_-245-13insTC