Canonical Allele Identifier: CA2346800335

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3916939_3916943delinsGATGA , CM000682.2:g.3916939_3916943delinsGATGA	GRCh38
NC_000020.10:g.3897586_3897590delinsGATGA , CM000682.1:g.3897586_3897590delinsGATGA	GRCh37
NC_000020.9:g.3845586_3845590delinsGATGA	NCBI36
NG_008131.3:g.33101_33105delinsGATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1095_1099delinsGATGA MANE Select	ENSP00000477429.2:p.Met365=
ENST00000316562.9:c.1425_1429delinsGATGA	ENSP00000313377.4:p.Met475=
ENST00000336066.8:c.*436_*440delinsGATGA	ENSP00000477229.2:n.*436_*440delinsGATGA
ENST00000610179.6:c.1095_1099delinsGATGA	ENSP00000477429.2:p.Met365=
ENST00000643504.2:c.*725_*729delinsGATGA	ENSP00000495157.2:n.*725_*729delinsGATGA
ENST00000646394.1:c.922_926delinsGATGA
ENST00000316562.8:c.1425_1429delinsGATGA	ENSP00000313377.4:p.Met475=
ENST00000336066.7:c.*436_*440delinsGATGA	ENSP00000477229.1:n.*436_*440delinsGATGA
ENST00000464452.1:n.660_664delinsGATGA
ENST00000495692.5:c.117_121delinsGATGA	ENSP00000476745.1:p.Met39=
ENST00000497424.5:c.552_556delinsGATGA	ENSP00000417609.1:p.Met184=
ENST00000610179.5:c.1056_1060delinsGATGA	ENSP00000477429.1:p.Met352=
ENST00000621507.1:c.552_556delinsGATGA	ENSP00000481523.1:p.Met184=
NM_024960.4:c.552_556delinsGATGA	NP_079236.3:p.Met184=
NM_153638.2:c.1425_1429delinsGATGA	NP_705902.2:p.Met475=
NM_153640.2:c.552_556delinsGATGA	NP_705904.1:p.Met184=
XM_005260835.2:c.810_814delinsGATGA	XP_005260892.1:p.Met270=
XM_005260836.3:c.552_556delinsGATGA	XP_005260893.3:p.Met184=
XM_006723631.1:c.552_556delinsGATGA	XP_006723694.1:p.Met184=
XM_011529364.1:c.1248_1252delinsGATGA	XP_011527666.1:p.Met416=
NM_001324191.1:c.552_556delinsGATGA	NP_001311120.1:p.Met184=
NM_001324193.1:c.117_121delinsGATGA	NP_001311122.1:p.Met39=
NM_024960.5:c.552_556delinsGATGA	NP_079236.3:p.Met184=
NM_153638.3:c.1425_1429delinsGATGA	NP_705902.2:p.Met475=
NM_153640.3:c.552_556delinsGATGA	NP_705904.1:p.Met184=
NR_136715.1:n.1449_1453delinsGATGA
XM_005260835.3:c.810_814delinsGATGA	XP_005260892.1:p.Met270=
XM_005260836.4:c.552_556delinsGATGA	XP_005260893.3:p.Met184=
XM_011529364.3:c.1248_1252delinsGATGA	XP_011527666.1:p.Met416=
XM_017028077.2:c.117_121delinsGATGA	XP_016883566.1:p.Met39=
XM_017028078.2:c.117_121delinsGATGA	XP_016883567.1:p.Met39=
XM_017028079.2:c.117_121delinsGATGA	XP_016883568.1:p.Met39=
XM_024452002.1:c.117_121delinsGATGA	XP_024307770.1:p.Met39=
XR_002958533.1:n.2213_2217delinsGATGA
NM_001324191.2:c.552_556delinsGATGA	NP_001311120.1:p.Met184=
NM_001324193.2:c.117_121delinsGATGA	NP_001311122.1:p.Met39=
NM_024960.6:c.552_556delinsGATGA	NP_079236.3:p.Met184=
NR_136715.2:n.996_1000delinsGATGA
NM_001386393.1:c.1095_1099delinsGATGA MANE Select	NP_001373322.1:p.Met365=
NM_153638.4:c.1425_1429delinsGATGA	NP_705902.2:p.Met475=
NM_153640.4:c.552_556delinsGATGA	NP_705904.1:p.Met184=