Canonical Allele Identifier: CA1205973280

Gene: ATP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169130112C= , CM000663.2:g.169130112C=	GRCh38
NC_000001.10:g.169099350C= , CM000663.1:g.169099350C=	GRCh37
NC_000001.9:g.167365974C=	NCBI36
NG_023230.1:g.28404C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494797.2:c.480+22C=	ENSP00000477015.2:n.480+22C=
ENST00000685155.1:c.480+22C=	ENSP00000508678.1:n.480+22C=
ENST00000685762.1:c.480+22C=	ENSP00000508918.1:n.480+22C=
ENST00000685792.1:c.480+22C=	ENSP00000508616.1:n.480+22C=
ENST00000686702.1:c.480+22C=	ENSP00000509060.1:n.480+22C=
ENST00000687013.1:n.4998+22C=
ENST00000687182.1:n.495+22C=
ENST00000687745.1:c.480+22C=	ENSP00000509323.1:n.480+22C=
ENST00000688406.1:n.3431C=
ENST00000688755.1:c.648+22C=	ENSP00000508725.1:n.648+22C=
ENST00000689522.1:c.648+22C=	ENSP00000509039.1:n.648+22C=
ENST00000690184.1:c.648+22C=	ENSP00000509517.1:n.648+22C=
ENST00000690604.1:n.2523+22C=
ENST00000691106.1:c.288+22C=	ENSP00000508710.1:n.288+22C=
ENST00000691753.1:c.480+22C=	ENSP00000509877.1:n.480+22C=
ENST00000691802.1:c.288+22C=	ENSP00000510565.1:n.288+22C=
ENST00000692003.1:n.3409+22C=
ENST00000367815.9:c.648+22C= MANE Select	ENSP00000356789.3:n.648+22C=
ENST00000367815.8:c.648+22C=	ENSP00000356789.3:n.648+22C=
ENST00000367816.5:c.648+22C=	ENSP00000356790.1:n.648+22C=
NM_001677.3:c.648+22C=	NP_001668.1:n.648+22C=
NM_001677.4:c.648+22C= MANE Select	NP_001668.1:n.648+22C=