Canonical Allele Identifier: CA1205973232
Gene: ATP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1658169243

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169129939_169129960del , CM000663.2:g.169129939_169129960del GRCh38
NC_000001.10:g.169099177_169099198del , CM000663.1:g.169099177_169099198del GRCh37
NC_000001.9:g.167365801_167365822del NCBI36
NG_023230.1:g.28231_28252del

Transcript Alleles

HGVS Amino-acid Change
ENST00000494797.2:c.400-71_400-50del ENSP00000477015.2:n.400-71_400-50del
ENST00000685155.1:c.400-71_400-50del ENSP00000508678.1:n.400-71_400-50del
ENST00000685762.1:c.400-71_400-50del ENSP00000508918.1:n.400-71_400-50del
ENST00000685792.1:c.400-71_400-50del ENSP00000508616.1:n.400-71_400-50del
ENST00000686702.1:c.400-71_400-50del ENSP00000509060.1:n.400-71_400-50del
ENST00000687013.1:n.4847_4868del
ENST00000687182.1:n.415-71_415-50del
ENST00000687745.1:c.400-71_400-50del ENSP00000509323.1:n.400-71_400-50del
ENST00000688406.1:n.3258_3279del
ENST00000688755.1:c.568-71_568-50del ENSP00000508725.1:n.568-71_568-50del
ENST00000689522.1:c.568-71_568-50del ENSP00000509039.1:n.568-71_568-50del
ENST00000690184.1:c.568-71_568-50del ENSP00000509517.1:n.568-71_568-50del
ENST00000690604.1:n.2443-71_2443-50del
ENST00000691106.1:c.208-71_208-50del ENSP00000508710.1:n.208-71_208-50del
ENST00000691753.1:c.400-71_400-50del ENSP00000509877.1:n.400-71_400-50del
ENST00000691802.1:c.208-71_208-50del ENSP00000510565.1:n.208-71_208-50del
ENST00000692003.1:n.3258_3279del
ENST00000367815.9:c.568-71_568-50del MANE Select ENSP00000356789.3:n.568-71_568-50del
ENST00000367815.8:c.568-71_568-50del ENSP00000356789.3:n.568-71_568-50del
ENST00000367816.5:c.568-71_568-50del ENSP00000356790.1:n.568-71_568-50del
NM_001677.3:c.568-71_568-50del NP_001668.1:n.568-71_568-50del
NM_001677.4:c.568-71_568-50del MANE Select NP_001668.1:n.568-71_568-50del