Canonical Allele Identifier: CA483126276

Gene: ATP8A2

Linked Data

• MyVariant Identifiers: chr13:g.26104177T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.25530039T>C , CM000675.2:g.25530039T>C	GRCh38
NC_000013.10:g.26104177T>C , CM000675.1:g.26104177T>C	GRCh37
NC_000013.9:g.25002177T>C	NCBI36
NG_042855.1:g.163029T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281620.11:c.262T>C	ENSP00000281620.7:p.Leu88=
ENST00000682472.1:c.262T>C	ENSP00000508103.1:p.Leu88=
ENST00000682580.1:n.214T>C
ENST00000682942.1:n.703T>C
ENST00000682943.1:c.222-2233T>C	ENSP00000507323.1:n.222-2233T>C
ENST00000683303.1:c.262T>C	ENSP00000508339.1:p.Leu88=
ENST00000683845.1:n.702T>C
ENST00000683945.1:n.174T>C
ENST00000683960.1:c.262T>C	ENSP00000506846.1:p.Leu88=
ENST00000684025.1:n.327T>C
ENST00000684283.1:c.262T>C	ENSP00000507994.1:p.Leu88=
ENST00000684424.1:c.142T>C	ENSP00000507489.1:p.Leu48=
ENST00000381655.7:c.262T>C MANE Select	ENSP00000371070.2:p.Leu88=
ENST00000255283.9:c.142T>C	ENSP00000255283.9:p.Leu48=
ENST00000281620.10:c.-209T>C	ENSP00000281620.6:n.-209T>C
ENST00000381648.7:n.186T>C
ENST00000381655.6:c.262T>C	ENSP00000371070.2:p.Leu88=
NM_001313741.1:c.142T>C	NP_001300670.1:p.Leu48=
NM_016529.4:c.262T>C	NP_057613.4:p.Leu88=
NM_016529.5:c.262T>C	NP_057613.4:p.Leu88=
XM_005266419.1:c.142T>C	XP_005266476.1:p.Leu48=
XM_011535103.1:c.262T>C	XP_011533405.1:p.Leu88=
XM_011535104.1:c.142T>C	XP_011533406.1:p.Leu48=
XM_011535106.1:c.262T>C	XP_011533408.1:p.Leu88=
XM_011535107.1:c.262T>C	XP_011533409.1:p.Leu88=
XM_011535108.1:c.-219T>C	XP_011533410.1:n.-219T>C
XM_011535109.1:c.-219T>C	XP_011533411.1:n.-219T>C
XM_011535110.1:c.-214T>C	XP_011533412.1:n.-214T>C
XM_011535111.1:c.-214T>C	XP_011533413.1:n.-214T>C
XM_011535112.1:c.-219T>C	XP_011533414.1:n.-219T>C
XM_011535113.1:c.262T>C	XP_011533415.1:p.Leu88=
XM_011535114.1:c.262T>C	XP_011533416.1:p.Leu88=
XM_011535104.3:c.142T>C	XP_011533406.1:p.Leu48=
XM_011535107.3:c.262T>C	XP_011533409.1:p.Leu88=
XM_011535109.3:c.-219T>C	XP_011533411.1:n.-219T>C
XM_011535113.2:c.262T>C	XP_011533415.1:p.Leu88=
XM_017020625.2:c.262T>C	XP_016876114.1:p.Leu88=
XM_017020626.1:c.262T>C	XP_016876115.1:p.Leu88=
NM_016529.6:c.262T>C MANE Select	NP_057613.4:p.Leu88=