Canonical Allele Identifier: CA15113112

Gene: ATP1B1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169119099A>C , CM000663.2:g.169119099A>C	GRCh38
NC_000001.10:g.169088337A>C , CM000663.1:g.169088337A>C	GRCh37
NC_000001.9:g.167354961A>C	NCBI36
NG_023230.1:g.17391A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494797.2:c.59-5785A>C	ENSP00000477015.2:n.59-5785A>C
ENST00000685155.1:c.59-5785A>C	ENSP00000508678.1:n.59-5785A>C
ENST00000685762.1:c.59-5785A>C	ENSP00000508918.1:n.59-5785A>C
ENST00000685792.1:c.59-5785A>C	ENSP00000508616.1:n.59-5785A>C
ENST00000686702.1:c.59-5785A>C	ENSP00000509060.1:n.59-5785A>C
ENST00000687182.1:n.73+2776A>C
ENST00000687745.1:c.59-5785A>C	ENSP00000509323.1:n.59-5785A>C
ENST00000688406.1:n.387-5785A>C
ENST00000688755.1:c.227-5785A>C	ENSP00000508725.1:n.227-5785A>C
ENST00000689522.1:c.227-5785A>C	ENSP00000509039.1:n.227-5785A>C
ENST00000690184.1:c.227-5785A>C	ENSP00000509517.1:n.227-5785A>C
ENST00000691106.1:c.-134-5785A>C	ENSP00000508710.1:n.-134-5785A>C
ENST00000691753.1:c.59-5785A>C	ENSP00000509877.1:n.59-5785A>C
ENST00000691802.1:c.-267-4538A>C	ENSP00000510565.1:n.-267-4538A>C
ENST00000692003.1:n.387-5785A>C
ENST00000367815.9:c.227-5785A>C MANE Select	ENSP00000356789.3:n.227-5785A>C
ENST00000367815.8:c.227-5785A>C	ENSP00000356789.3:n.227-5785A>C
ENST00000367816.5:c.227-5785A>C	ENSP00000356790.1:n.227-5785A>C
ENST00000494797.1:c.59-5785A>C	ENSP00000477015.1:n.59-5785A>C
NM_001677.3:c.227-5785A>C	NP_001668.1:n.227-5785A>C
NM_001677.4:c.227-5785A>C MANE Select	NP_001668.1:n.227-5785A>C