Canonical Allele Identifier: CA408122660
Community Standard Title: NM_001386393.1(PANK2):c.1336T>C (p.Tyr446His)
Gene: PANK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3923247T>C , CM000682.2:g.3923247T>C GRCh38
NC_000020.10:g.3903894T>C , CM000682.1:g.3903894T>C GRCh37
NC_000020.9:g.3851894T>C NCBI36
NG_008131.3:g.39409T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001386393.1:c.1336T>C MANE Select NP_001373322.1:p.Tyr446His
ENST00000610179.7:c.1336T>C MANE Select ENSP00000477429.2:p.Tyr446His
NM_001324191.1:c.793T>C NP_001311120.1:p.Tyr265His
NM_001324191.2:c.793T>C NP_001311120.1:p.Tyr265His
NM_001324193.1:c.358T>C NP_001311122.1:p.Tyr120His
NM_001324193.2:c.358T>C NP_001311122.1:p.Tyr120His
NM_024960.4:c.793T>C NP_079236.3:p.Tyr265His
NM_024960.5:c.793T>C NP_079236.3:p.Tyr265His
NM_024960.6:c.793T>C NP_079236.3:p.Tyr265His
NM_153638.2:c.1666T>C NP_705902.2:p.Tyr556His
NM_153638.3:c.1666T>C NP_705902.2:p.Tyr556His
NM_153638.4:c.1666T>C NP_705902.2:p.Tyr556His
NM_153640.2:c.793T>C NP_705904.1:p.Tyr265His
NM_153640.3:c.793T>C NP_705904.1:p.Tyr265His
NM_153640.4:c.793T>C NP_705904.1:p.Tyr265His
NR_136715.1:n.1690T>C
NR_136715.2:n.1237T>C
ENST00000316562.8:c.1666T>C ENSP00000313377.4:p.Tyr556His
ENST00000316562.9:c.1666T>C ENSP00000313377.4:p.Tyr556His
ENST00000336066.7:c.*677T>C ENSP00000477229.1:n.*677T>C
ENST00000336066.8:c.*677T>C ENSP00000477229.2:n.*677T>C
ENST00000497424.5:c.793T>C ENSP00000417609.1:p.Tyr265His
ENST00000610179.5:c.1297T>C ENSP00000477429.1:p.Tyr433His
ENST00000610179.6:c.1336T>C ENSP00000477429.2:p.Tyr446His
ENST00000621507.1:c.793T>C ENSP00000481523.1:p.Tyr265His
ENST00000643504.2:c.*966T>C ENSP00000495157.2:n.*966T>C
ENST00000646394.1:c.1163T>C
XM_005260835.2:c.1051T>C XP_005260892.1:p.Tyr351His
XM_005260835.3:c.1051T>C XP_005260892.1:p.Tyr351His
XM_005260836.3:c.793T>C XP_005260893.3:p.Tyr265His
XM_005260836.4:c.793T>C XP_005260893.3:p.Tyr265His
XM_006723631.1:c.793T>C XP_006723694.1:p.Tyr265His
XM_011529364.1:c.1489T>C XP_011527666.1:p.Tyr497His
XM_011529364.3:c.1489T>C XP_011527666.1:p.Tyr497His
XM_017028077.2:c.358T>C XP_016883566.1:p.Tyr120His
XM_017028078.2:c.358T>C XP_016883567.1:p.Tyr120His
XM_017028079.2:c.358T>C XP_016883568.1:p.Tyr120His
XM_024452002.1:c.358T>C XP_024307770.1:p.Tyr120His
XR_002958533.1:n.2454T>C