Canonical Allele Identifier: CA351781303

Gene: ATP2B2

Linked Data

• MyVariant Identifiers: chr3:g.10401640C>A (hg19) ; chr3:g.10359956C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10359956C>A , CM000665.2:g.10359956C>A	GRCh38
NC_000003.11:g.10401640C>A , CM000665.1:g.10401640C>A	GRCh37
NC_000003.10:g.10376640C>A	NCBI36
NG_012046.1:g.150629G>T
NG_012046.2:g.353076G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644807.2:c.1692G>T	ENSP00000495228.1:p.Met564Ile
ENST00000352432.9:c.1794G>T	ENSP00000324172.6:p.Met598Ile
ENST00000360273.7:c.1827G>T MANE Select	ENSP00000353414.2:p.Met609Ile
ENST00000397077.6:c.1692G>T	ENSP00000380267.1:p.Met564Ile
ENST00000452124.2:c.1734G>T	ENSP00000414854.2:p.Met578Ile
ENST00000638646.2:c.1692G>T	ENSP00000492732.2:p.Met564Ile
ENST00000643662.1:c.1734G>T	ENSP00000495924.1:p.Met578Ile
ENST00000644553.1:c.1086G>T	ENSP00000494004.1:p.Met362Ile
ENST00000644807.1:c.1692G>T	ENSP00000495228.1:p.Met564Ile
ENST00000645850.1:c.1827G>T	ENSP00000494716.1:p.Met609Ile
ENST00000646379.1:c.1692G>T	ENSP00000494381.1:p.Met564Ile
ENST00000352432.8:c.1827G>T	ENSP00000324172.5:p.Met609Ile
ENST00000360273.6:c.1827G>T	ENSP00000353414.2:p.Met609Ile
ENST00000383800.8:c.1692G>T	ENSP00000373311.4:p.Met564Ile
ENST00000397077.5:c.1692G>T	ENSP00000380267.1:p.Met564Ile
ENST00000452124.1:c.1395G>T	ENSP00000414854.1:p.Met465Ile
ENST00000460129.5:c.1692G>T	ENSP00000424494.1:p.Met564Ile
NM_001001331.2:c.1827G>T	NP_001001331.1:p.Met609Ile
NM_001683.3:c.1692G>T	NP_001674.2:p.Met564Ile
XM_005265179.3:c.1827G>T	XP_005265236.1:p.Met609Ile
XM_006713175.2:c.1827G>T	XP_006713238.1:p.Met609Ile
XM_011533751.1:c.1827G>T	XP_011532053.1:p.Met609Ile
XM_011533752.1:c.1827G>T	XP_011532054.1:p.Met609Ile
XM_011533753.1:c.1794G>T	XP_011532055.1:p.Met598Ile
XM_011533754.1:c.1734G>T	XP_011532056.1:p.Met578Ile
XM_011533755.1:c.1827G>T	XP_011532057.1:p.Met609Ile
XM_011533756.1:c.1827G>T	XP_011532058.1:p.Met609Ile
XM_011533757.1:c.1692G>T	XP_011532059.1:p.Met564Ile
XM_011533758.1:c.1734G>T	XP_011532060.1:p.Met578Ile
XM_011533759.1:c.759G>T	XP_011532061.1:p.Met253Ile
NM_001001331.3:c.1827G>T	NP_001001331.1:p.Met609Ile
NM_001330611.2:c.1692G>T	NP_001317540.1:p.Met564Ile
NM_001353564.1:c.1692G>T	NP_001340493.1:p.Met564Ile
NM_001363862.1:c.1692G>T	NP_001350791.1:p.Met564Ile
NM_001683.4:c.1692G>T	NP_001674.2:p.Met564Ile
XM_005265179.5:c.1827G>T	XP_005265236.1:p.Met609Ile
XM_006713175.4:c.1827G>T	XP_006713238.1:p.Met609Ile
XM_011533752.3:c.1827G>T	XP_011532054.1:p.Met609Ile
XM_017006481.2:c.1827G>T	XP_016861970.1:p.Met609Ile
XM_017006482.2:c.1827G>T	XP_016861971.1:p.Met609Ile
XM_017006483.2:c.1734G>T	XP_016861972.1:p.Met578Ile
XM_017006484.2:c.1734G>T	XP_016861973.1:p.Met578Ile
XM_017006485.2:c.1827G>T	XP_016861974.1:p.Met609Ile
XM_017006486.2:c.1827G>T	XP_016861975.1:p.Met609Ile
XM_017006487.1:c.1692G>T	XP_016861976.1:p.Met564Ile
XM_017006488.2:c.1734G>T	XP_016861977.1:p.Met578Ile
XM_017006489.2:c.1734G>T	XP_016861978.1:p.Met578Ile
XM_017006492.2:c.1827G>T	XP_016861981.1:p.Met609Ile
NM_001001331.4:c.1827G>T MANE Select	NP_001001331.1:p.Met609Ile
NM_001330611.3:c.1692G>T	NP_001317540.1:p.Met564Ile
NM_001683.5:c.1692G>T	NP_001674.2:p.Met564Ile