Canonical Allele Identifier: CA1202192959

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130396_160130397delinsCA , CM000663.2:g.160130396_160130397delinsCA	GRCh38
NC_000001.10:g.160100186_160100187delinsCA , CM000663.1:g.160100186_160100187delinsCA	GRCh37
NC_000001.9:g.158366810_158366811delinsCA	NCBI36
NG_008014.1:g.19639_19640delinsCA , LRG_6:g.19639_19640delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.1652-26_1652-25delinsCA MANE Select	ENSP00000354490.3:n.1652-26_1652-25delinsCA
ENST00000361216.7:c.1652-26_1652-25delinsCA	ENSP00000354490.3:n.1652-26_1652-25delinsCA
ENST00000392233.7:c.1652-26_1652-25delinsCA	ENSP00000376066.3:n.1652-26_1652-25delinsCA
ENST00000447527.1:c.784-26_784-25delinsCA
ENST00000472488.5:n.1755-26_1755-25delinsCA
NM_000702.3:c.1652-26_1652-25delinsCA	NP_000693.1:n.1652-26_1652-25delinsCA
NM_000702.4:c.1652-26_1652-25delinsCA MANE Select	NP_000693.1:n.1652-26_1652-25delinsCA