Canonical Allele Identifier: CA2079675469
Gene: ATP8A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.25529998G= , CM000675.2:g.25529998G= GRCh38
NC_000013.10:g.26104136G= , CM000675.1:g.26104136G= GRCh37
NC_000013.9:g.25002136G= NCBI36
NG_042855.1:g.162988G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281620.11:c.222-1G= ENSP00000281620.7:n.222-1G=
ENST00000682472.1:c.222-1G= ENSP00000508103.1:n.222-1G=
ENST00000682580.1:n.174-1G=
ENST00000682942.1:n.663-1G=
ENST00000682943.1:c.222-2274G= ENSP00000507323.1:n.222-2274G=
ENST00000683303.1:c.222-1G= ENSP00000508339.1:n.222-1G=
ENST00000683845.1:n.662-1G=
ENST00000683945.1:n.134-1G=
ENST00000683960.1:c.222-1G= ENSP00000506846.1:n.222-1G=
ENST00000684025.1:n.287-1G=
ENST00000684283.1:c.222-1G= ENSP00000507994.1:n.222-1G=
ENST00000684424.1:c.102-1G= ENSP00000507489.1:n.102-1G=
ENST00000381655.7:c.222-1G= MANE Select ENSP00000371070.2:n.222-1G=
ENST00000255283.9:c.102-1G= ENSP00000255283.9:n.102-1G=
ENST00000281620.10:c.-249-1G= ENSP00000281620.6:n.-249-1G=
ENST00000381648.7:n.146-1G=
ENST00000381655.6:c.222-1G= ENSP00000371070.2:n.222-1G=
NM_001313741.1:c.102-1G= NP_001300670.1:n.102-1G=
NM_016529.4:c.222-1G= NP_057613.4:n.222-1G=
NM_016529.5:c.222-1G= NP_057613.4:n.222-1G=
XM_005266419.1:c.102-1G= XP_005266476.1:n.102-1G=
XM_011535103.1:c.222-1G= XP_011533405.1:n.222-1G=
XM_011535104.1:c.102-1G= XP_011533406.1:n.102-1G=
XM_011535106.1:c.222-1G= XP_011533408.1:n.222-1G=
XM_011535107.1:c.222-1G= XP_011533409.1:n.222-1G=
XM_011535108.1:c.-259-1G= XP_011533410.1:n.-259-1G=
XM_011535109.1:c.-259-1G= XP_011533411.1:n.-259-1G=
XM_011535110.1:c.-254-1G= XP_011533412.1:n.-254-1G=
XM_011535111.1:c.-254-1G= XP_011533413.1:n.-254-1G=
XM_011535112.1:c.-259-1G= XP_011533414.1:n.-259-1G=
XM_011535113.1:c.222-1G= XP_011533415.1:n.222-1G=
XM_011535114.1:c.222-1G= XP_011533416.1:n.222-1G=
XM_011535104.3:c.102-1G= XP_011533406.1:n.102-1G=
XM_011535107.3:c.222-1G= XP_011533409.1:n.222-1G=
XM_011535109.3:c.-259-1G= XP_011533411.1:n.-259-1G=
XM_011535113.2:c.222-1G= XP_011533415.1:n.222-1G=
XM_017020625.2:c.222-1G= XP_016876114.1:n.222-1G=
XM_017020626.1:c.222-1G= XP_016876115.1:n.222-1G=
NM_016529.6:c.222-1G= MANE Select NP_057613.4:n.222-1G=