Canonical Allele Identifier: CA2574635194
Gene: HPSE2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.98489952G>T , CM000672.2:g.98489952G>T GRCh38
NC_000010.10:g.100249709G>T , CM000672.1:g.100249709G>T GRCh37
NC_000010.9:g.100239699G>T NCBI36
NG_023416.1:g.750924C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370552.8:c.1466+99C>A MANE Select ENSP00000359583.3:n.1466+99C>A
ENST00000370546.5:c.1466+99C>A ENSP00000359577.1:n.1466+99C>A
ENST00000370549.5:c.1292+99C>A ENSP00000359580.1:n.1292+99C>A
ENST00000370552.7:c.1466+99C>A ENSP00000359583.3:n.1466+99C>A
ENST00000404542.5:c.857+99C>A ENSP00000384384.2:n.857+99C>A
ENST00000628193.2:c.1130+99C>A ENSP00000485916.1:n.1130+99C>A
NM_001166244.1:c.1292+99C>A NP_001159716.1:n.1292+99C>A
NM_001166245.1:c.1130+99C>A NP_001159717.1:n.1130+99C>A
NM_001166246.1:c.1466+99C>A NP_001159718.1:n.1466+99C>A
NM_021828.4:c.1466+99C>A NP_068600.4:n.1466+99C>A
XM_006717937.2:c.950+99C>A XP_006718000.1:n.950+99C>A
XM_011540029.1:c.1466+99C>A XP_011538331.1:n.1466+99C>A
XM_011540030.1:c.1304+99C>A XP_011538332.1:n.1304+99C>A
XM_011540031.1:c.950+99C>A XP_011538333.1:n.950+99C>A
XM_011540033.1:c.662+99C>A XP_011538335.1:n.662+99C>A
XR_945794.1:n.1539+99C>A
XM_011540031.2:c.950+99C>A XP_011538333.1:n.950+99C>A
XM_017016495.1:c.1466+99C>A XP_016871984.1:n.1466+99C>A
XM_017016497.1:c.950+99C>A XP_016871986.1:n.950+99C>A
XM_017016498.1:c.662+99C>A XP_016871987.1:n.662+99C>A
XM_024448119.1:c.950+99C>A XP_024303887.1:n.950+99C>A
XM_024448120.1:c.662+99C>A XP_024303888.1:n.662+99C>A
XR_001747170.1:n.1543+99C>A
NM_021828.5:c.1466+99C>A MANE Select NP_068600.4:n.1466+99C>A