Canonical Allele Identifier: CA1205973263

Gene: ATP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169130035C= , CM000663.2:g.169130035C=	GRCh38
NC_000001.10:g.169099273C= , CM000663.1:g.169099273C=	GRCh37
NC_000001.9:g.167365897C=	NCBI36
NG_023230.1:g.28327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494797.2:c.425C=	ENSP00000477015.2:p.Thr142=
ENST00000685155.1:c.425C=	ENSP00000508678.1:p.Thr142=
ENST00000685762.1:c.425C=	ENSP00000508918.1:p.Thr142=
ENST00000685792.1:c.425C=	ENSP00000508616.1:p.Thr142=
ENST00000686702.1:c.425C=	ENSP00000509060.1:p.Thr142=
ENST00000687013.1:n.4943C=
ENST00000687182.1:n.440C=
ENST00000687745.1:c.425C=	ENSP00000509323.1:p.Thr142=
ENST00000688406.1:n.3354C=
ENST00000688755.1:c.593C=	ENSP00000508725.1:p.Thr198=
ENST00000689522.1:c.593C=	ENSP00000509039.1:p.Thr198=
ENST00000690184.1:c.593C=	ENSP00000509517.1:p.Thr198=
ENST00000690604.1:n.2468C=
ENST00000691106.1:c.233C=	ENSP00000508710.1:p.Thr78=
ENST00000691753.1:c.425C=	ENSP00000509877.1:p.Thr142=
ENST00000691802.1:c.233C=	ENSP00000510565.1:p.Thr78=
ENST00000692003.1:n.3354C=
ENST00000367815.9:c.593C= MANE Select	ENSP00000356789.3:p.Thr198=
ENST00000367815.8:c.593C=	ENSP00000356789.3:p.Thr198=
ENST00000367816.5:c.593C=	ENSP00000356790.1:p.Thr198=
NM_001677.3:c.593C=	NP_001668.1:p.Thr198=
NM_001677.4:c.593C= MANE Select	NP_001668.1:p.Thr198=