Canonical Allele Identifier: CA1345250996

Gene: ATP2B2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10494087C= , CM000665.2:g.10494087C=	GRCh38
NC_000003.11:g.10535771C= , CM000665.1:g.10535771C=	GRCh37
NC_000003.10:g.10510771C=	NCBI36
NG_012046.1:g.16498G=
NG_012046.2:g.218945G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644807.2:c.-320+11378G=	ENSP00000495228.1:n.-320+11378G=
ENST00000360273.7:c.-320+11378G= MANE Select	ENSP00000353414.2:n.-320+11378G=
ENST00000397077.6:c.-320+11378G=	ENSP00000380267.1:n.-320+11378G=
ENST00000643662.1:c.-320+11378G=	ENSP00000495924.1:n.-320+11378G=
ENST00000646379.1:c.-320+39952G=	ENSP00000494381.1:n.-320+39952G=
ENST00000360273.6:c.-320+11378G=	ENSP00000353414.2:n.-320+11378G=
ENST00000383800.8:c.-320+11378G=	ENSP00000373311.4:n.-320+11378G=
ENST00000397077.5:c.-320+39952G=	ENSP00000380267.1:n.-320+39952G=
ENST00000460129.5:c.-320+39952G=	ENSP00000424494.1:n.-320+39952G=
ENST00000480680.2:n.120+11378G=
NM_001001331.2:c.-320+11378G=	NP_001001331.1:n.-320+11378G=
NM_001683.3:c.-320+11378G=	NP_001674.2:n.-320+11378G=
XM_005265179.3:c.-320+39952G=	XP_005265236.1:n.-320+39952G=
XM_006713175.2:c.-320+39952G=	XP_006713238.1:n.-320+39952G=
XM_011533751.1:c.-320+39952G=	XP_011532053.1:n.-320+39952G=
XM_011533752.1:c.-320+33659G=	XP_011532054.1:n.-320+33659G=
XM_011533753.1:c.-320+39952G=	XP_011532055.1:n.-320+39952G=
XM_011533754.1:c.-320+39952G=	XP_011532056.1:n.-320+39952G=
XM_011533755.1:c.-320+39952G=	XP_011532057.1:n.-320+39952G=
XM_011533756.1:c.-320+39952G=	XP_011532058.1:n.-320+39952G=
XM_011533757.1:c.-320+39952G=	XP_011532059.1:n.-320+39952G=
XM_011533758.1:c.-320+39952G=	XP_011532060.1:n.-320+39952G=
NM_001001331.3:c.-320+11378G=	NP_001001331.1:n.-320+11378G=
NM_001330611.2:c.-320+11378G=	NP_001317540.1:n.-320+11378G=
NM_001353564.1:c.-320+39952G=	NP_001340493.1:n.-320+39952G=
NM_001363862.1:c.-320+11378G=	NP_001350791.1:n.-320+11378G=
NM_001683.4:c.-320+11378G=	NP_001674.2:n.-320+11378G=
XM_005265179.5:c.-320+39952G=	XP_005265236.1:n.-320+39952G=
XM_006713175.4:c.-320+39952G=	XP_006713238.1:n.-320+39952G=
XM_011533752.3:c.-320+33659G=	XP_011532054.1:n.-320+33659G=
XM_017006481.2:c.-320+39952G=	XP_016861970.1:n.-320+39952G=
XM_017006483.2:c.-320+11378G=	XP_016861972.1:n.-320+11378G=
XM_017006484.2:c.-320+39952G=	XP_016861973.1:n.-320+39952G=
XM_017006485.2:c.-320+11378G=	XP_016861974.1:n.-320+11378G=
XM_017006486.2:c.-320+11378G=	XP_016861975.1:n.-320+11378G=
XM_017006487.1:c.-320+39952G=	XP_016861976.1:n.-320+39952G=
XM_017006488.2:c.-320+11378G=	XP_016861977.1:n.-320+11378G=
XM_017006489.2:c.-320+11378G=	XP_016861978.1:n.-320+11378G=
XM_017006492.2:c.-320+11378G=	XP_016861981.1:n.-320+11378G=
NM_001001331.4:c.-320+11378G= MANE Select	NP_001001331.1:n.-320+11378G=
NM_001330611.3:c.-320+11378G=	NP_001317540.1:n.-320+11378G=
NM_001683.5:c.-320+11378G=	NP_001674.2:n.-320+11378G=