Canonical Allele Identifier: CA2815082498

Gene: PANK2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3912631_3912632insG , CM000682.2:g.3912631_3912632insG	GRCh38
NC_000020.10:g.3893278_3893279insG , CM000682.1:g.3893278_3893279insG	GRCh37
NC_000020.9:g.3841278_3841279insG	NCBI36
NG_008131.3:g.28793_28794insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610179.7:c.1079_1080insG MANE Select	ENSP00000477429.2:p.Ser361LysfsTer16
ENST00000316562.9:c.1409_1410insG	ENSP00000313377.4:p.Ser471LysfsTer16
ENST00000336066.8:c.*420_*421insG	ENSP00000477229.2:n.*420_*421insG
ENST00000610179.6:c.1079_1080insG	ENSP00000477429.2:p.Ser361LysfsTer16
ENST00000643504.2:c.*709_*710insG	ENSP00000495157.2:n.*709_*710insG
ENST00000646394.1:c.906_907insG
ENST00000316562.8:c.1409_1410insG	ENSP00000313377.4:p.Ser471LysfsTer16
ENST00000336066.7:c.*420_*421insG	ENSP00000477229.1:n.*420_*421insG
ENST00000464452.1:n.644_645insG
ENST00000495692.5:c.101_102insG	ENSP00000476745.1:p.Ser35LysfsTer16
ENST00000497424.5:c.536_537insG	ENSP00000417609.1:p.Ser180LysfsTer16
ENST00000610179.5:c.1040_1041insG	ENSP00000477429.1:p.Ser348LysfsTer16
ENST00000621507.1:c.536_537insG	ENSP00000481523.1:p.Ser180LysfsTer16
NM_024960.4:c.536_537insG	NP_079236.3:p.Ser180LysfsTer16
NM_153638.2:c.1409_1410insG	NP_705902.2:p.Ser471LysfsTer16
NM_153640.2:c.536_537insG	NP_705904.1:p.Ser180LysfsTer16
XM_005260835.2:c.794_795insG	XP_005260892.1:p.Ser266LysfsTer16
XM_005260836.3:c.536_537insG	XP_005260893.3:p.Ser180LysfsTer16
XM_006723631.1:c.536_537insG	XP_006723694.1:p.Ser180LysfsTer16
XM_011529364.1:c.1235+1801_1235+1802insG	XP_011527666.1:n.1235+1801_1235+1802insG
NM_001324191.1:c.536_537insG	NP_001311120.1:p.Ser180LysfsTer16
NM_001324193.1:c.101_102insG	NP_001311122.1:p.Ser35LysfsTer16
NM_024960.5:c.536_537insG	NP_079236.3:p.Ser180LysfsTer16
NM_153638.3:c.1409_1410insG	NP_705902.2:p.Ser471LysfsTer16
NM_153640.3:c.536_537insG	NP_705904.1:p.Ser180LysfsTer16
NR_136715.1:n.1433_1434insG
XM_005260835.3:c.794_795insG	XP_005260892.1:p.Ser266LysfsTer16
XM_005260836.4:c.536_537insG	XP_005260893.3:p.Ser180LysfsTer16
XM_011529364.3:c.1235+1801_1235+1802insG	XP_011527666.1:n.1235+1801_1235+1802insG
XM_017028077.2:c.101_102insG	XP_016883566.1:p.Ser35LysfsTer16
XM_017028078.2:c.101_102insG	XP_016883567.1:p.Ser35LysfsTer16
XM_017028079.2:c.101_102insG	XP_016883568.1:p.Ser35LysfsTer16
XM_024452002.1:c.101_102insG	XP_024307770.1:p.Ser35LysfsTer16
XR_002958533.1:n.2197_2198insG
NM_001324191.2:c.536_537insG	NP_001311120.1:p.Ser180LysfsTer16
NM_001324193.2:c.101_102insG	NP_001311122.1:p.Ser35LysfsTer16
NM_024960.6:c.536_537insG	NP_079236.3:p.Ser180LysfsTer16
NR_136715.2:n.980_981insG
NM_001386393.1:c.1079_1080insG MANE Select	NP_001373322.1:p.Ser361LysfsTer16
NM_153638.4:c.1409_1410insG	NP_705902.2:p.Ser471LysfsTer16
NM_153640.4:c.536_537insG	NP_705904.1:p.Ser180LysfsTer16