Canonical Allele Identifier: CA2053627867

Gene: ATP2B1

Linked Data

• dbSNP Id: rs1878756024

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.89615262_89615263del , CM000674.2:g.89615262_89615263del	GRCh38
NC_000012.11:g.90009039_90009040del , CM000674.1:g.90009039_90009040del	GRCh37
NC_000012.10:g.88533170_88533171del	NCBI36
NG_029485.1:g.45811_45812del
NG_029485.2:g.99097_99098del

Transcript Alleles

HGVS	Amino-acid change
ENST00000359142.8:c.2067+1545_2067+1546del	ENSP00000352054.3:n.2067+1545_2067+1546de...
ENST00000551310.2:c.2067+1545_2067+1546del	ENSP00000447041.2:n.2067+1545_2067+1546de...
ENST00000705822.1:c.2067+1545_2067+1546del	ENSP00000516172.1:n.2067+1545_2067+1546de...
ENST00000428670.8:c.2067+1545_2067+1546del MANE Select	ENSP00000392043.3:n.2067+1545_2067+1546de...
ENST00000261173.6:c.2067+1545_2067+1546del	ENSP00000261173.2:n.2067+1545_2067+1546de...
ENST00000359142.7:c.2067+1545_2067+1546del	ENSP00000352054.3:n.2067+1545_2067+1546de...
ENST00000393164.6:c.1296+1545_1296+1546del	ENSP00000376869.2:n.1296+1545_1296+1546de...
ENST00000428670.7:c.2067+1545_2067+1546del	ENSP00000392043.3:n.2067+1545_2067+1546de...
NM_001001323.1:c.2067+1545_2067+1546del	NP_001001323.1:n.2067+1545_2067+1546del
NM_001682.2:c.2067+1545_2067+1546del	NP_001673.2:n.2067+1545_2067+1546del
XM_005268919.1:c.2067+1545_2067+1546del	XP_005268976.1:n.2067+1545_2067+1546del
XM_011538407.1:c.2067+1545_2067+1546del	XP_011536709.1:n.2067+1545_2067+1546del
XM_011538408.1:c.2067+1545_2067+1546del	XP_011536710.1:n.2067+1545_2067+1546del
XM_011538409.1:c.2067+1545_2067+1546del	XP_011536711.1:n.2067+1545_2067+1546del
XM_011538410.1:c.2067+1545_2067+1546del	XP_011536712.1:n.2067+1545_2067+1546del
XM_011538411.1:c.2067+1545_2067+1546del	XP_011536713.1:n.2067+1545_2067+1546del
XM_011538412.1:c.2067+1545_2067+1546del	XP_011536714.1:n.2067+1545_2067+1546del
XR_944556.1:n.2529+1545_2529+1546del
NM_001001323.2:c.2067+1545_2067+1546del	NP_001001323.1:n.2067+1545_2067+1546del
NM_001366520.1:c.2067+1545_2067+1546del	NP_001353449.1:n.2067+1545_2067+1546del
NM_001366521.1:c.2067+1545_2067+1546del MANE Select	NP_001353450.1:n.2067+1545_2067+1546del
NM_001366522.1:c.2067+1545_2067+1546del	NP_001353451.1:n.2067+1545_2067+1546del
NM_001366523.1:c.2067+1545_2067+1546del	NP_001353452.1:n.2067+1545_2067+1546del
NM_001366524.1:c.2067+1545_2067+1546del	NP_001353453.1:n.2067+1545_2067+1546del
NM_001366525.1:c.2067+1545_2067+1546del	NP_001353454.1:n.2067+1545_2067+1546del
NM_001366526.1:c.2067+1545_2067+1546del	NP_001353455.1:n.2067+1545_2067+1546del
NM_001366527.1:c.2067+1545_2067+1546del	NP_001353456.1:n.2067+1545_2067+1546del
NM_001366528.1:c.2067+1545_2067+1546del	NP_001353457.1:n.2067+1545_2067+1546del
NM_001366529.1:c.2067+1545_2067+1546del	NP_001353458.1:n.2067+1545_2067+1546del
NM_001366530.1:c.1869+1545_1869+1546del	NP_001353459.1:n.1869+1545_1869+1546del
NM_001366531.1:c.1506+1545_1506+1546del	NP_001353460.1:n.1506+1545_1506+1546del
NM_001366532.1:c.1506+1545_1506+1546del	NP_001353461.1:n.1506+1545_1506+1546del
NM_001682.3:c.2067+1545_2067+1546del	NP_001673.2:n.2067+1545_2067+1546del
XM_017019357.2:c.2067+1545_2067+1546del	XP_016874846.1:n.2067+1545_2067+1546del
XM_024448991.1:c.2067+1545_2067+1546del	XP_024304759.1:n.2067+1545_2067+1546del
XM_024448993.1:c.2067+1545_2067+1546del	XP_024304761.1:n.2067+1545_2067+1546del
XR_002957330.1:n.2529+1545_2529+1546del