Canonical Allele Identifier: CA645530211

Gene: ATP1B1

Linked Data

• COSMIC: COSM1745447

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169130054_169130056dup , CM000663.2:g.169130054_169130056dup	GRCh38
NC_000001.10:g.169099292_169099294dup , CM000663.1:g.169099292_169099294dup	GRCh37
NC_000001.9:g.167365916_167365918dup	NCBI36
NG_023230.1:g.28346_28348dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494797.2:c.444_446dup	ENSP00000477015.2:p.Asn149_Pro150insAsn
ENST00000685155.1:c.444_446dup	ENSP00000508678.1:p.Asn149_Pro150insAsn
ENST00000685762.1:c.444_446dup	ENSP00000508918.1:p.Asn149_Pro150insAsn
ENST00000685792.1:c.444_446dup	ENSP00000508616.1:p.Asn149_Pro150insAsn
ENST00000686702.1:c.444_446dup	ENSP00000509060.1:p.Asn149_Pro150insAsn
ENST00000687013.1:n.4962_4964dup
ENST00000687182.1:n.459_461dup
ENST00000687745.1:c.444_446dup	ENSP00000509323.1:p.Asn149_Pro150insAsn
ENST00000688406.1:n.3373_3375dup
ENST00000688755.1:c.612_614dup	ENSP00000508725.1:p.Asn205_Pro206insAsn
ENST00000689522.1:c.612_614dup	ENSP00000509039.1:p.Asn205_Pro206insAsn
ENST00000690184.1:c.612_614dup	ENSP00000509517.1:p.Asn205_Pro206insAsn
ENST00000690604.1:n.2487_2489dup
ENST00000691106.1:c.252_254dup	ENSP00000508710.1:p.Asn85_Pro86insAsn
ENST00000691753.1:c.444_446dup	ENSP00000509877.1:p.Asn149_Pro150insAsn
ENST00000691802.1:c.252_254dup	ENSP00000510565.1:p.Asn85_Pro86insAsn
ENST00000692003.1:n.3373_3375dup
ENST00000367815.9:c.612_614dup MANE Select	ENSP00000356789.3:p.Asn205_Pro206insAsn
ENST00000367815.8:c.612_614dup	ENSP00000356789.3:p.Asn205_Pro206insAsn
ENST00000367816.5:c.612_614dup	ENSP00000356790.1:p.Asn205_Pro206insAsn
NM_001677.3:c.612_614dup	NP_001668.1:p.Asn205_Pro206insAsn
NM_001677.4:c.612_614dup MANE Select	NP_001668.1:p.Asn205_Pro206insAsn