Canonical Allele Identifier: CA2649020896
Gene: ATP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169130175del , CM000663.2:g.169130175del GRCh38
NC_000001.10:g.169099413del , CM000663.1:g.169099413del GRCh37
NC_000001.9:g.167366037del NCBI36
NG_023230.1:g.28467del

Transcript Alleles

HGVS Amino-acid change
ENST00000494797.2:c.480+85del ENSP00000477015.2:n.480+85del
ENST00000685155.1:c.480+85del ENSP00000508678.1:n.480+85del
ENST00000685762.1:c.480+85del ENSP00000508918.1:n.480+85del
ENST00000685792.1:c.480+85del ENSP00000508616.1:n.480+85del
ENST00000686702.1:c.480+85del ENSP00000509060.1:n.480+85del
ENST00000687013.1:n.4998+85del
ENST00000687182.1:n.495+85del
ENST00000687745.1:c.480+85del ENSP00000509323.1:n.480+85del
ENST00000688406.1:n.3494del
ENST00000688755.1:c.648+85del ENSP00000508725.1:n.648+85del
ENST00000689522.1:c.648+85del ENSP00000509039.1:n.648+85del
ENST00000690184.1:c.648+85del ENSP00000509517.1:n.648+85del
ENST00000690604.1:n.2523+85del
ENST00000691106.1:c.288+85del ENSP00000508710.1:n.288+85del
ENST00000691753.1:c.480+85del ENSP00000509877.1:n.480+85del
ENST00000691802.1:c.288+85del ENSP00000510565.1:n.288+85del
ENST00000692003.1:n.3409+85del
ENST00000367815.9:c.648+85del MANE Select ENSP00000356789.3:n.648+85del
ENST00000367815.8:c.648+85del ENSP00000356789.3:n.648+85del
ENST00000367816.5:c.648+85del ENSP00000356790.1:n.648+85del
NM_001677.3:c.648+85del NP_001668.1:n.648+85del
NM_001677.4:c.648+85del MANE Select NP_001668.1:n.648+85del