Canonical Allele Identifier: CA1202196776

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139467_160139471delinsCAAAT , CM000663.2:g.160139467_160139471delinsCAAAT	GRCh38
NC_000001.10:g.160109257_160109261delinsCAAAT , CM000663.1:g.160109257_160109261delinsCAAAT	GRCh37
NC_000001.9:g.158375881_158375885delinsCAAAT	NCBI36
NG_008014.1:g.28710_28714delinsCAAAT , LRG_6:g.28710_28714delinsCAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.2841-173_2841-169delinsCAAAT MANE Select	ENSP00000354490.3:n.2841-173_2841-169delinsCAAAT
ENST00000361216.7:c.2841-173_2841-169delinsCAAAT	ENSP00000354490.3:n.2841-173_2841-169delinsCAAAT
ENST00000392233.7:c.2841-173_2841-169delinsCAAAT	ENSP00000376066.3:n.2841-173_2841-169delinsCAAAT
ENST00000447527.1:c.1922-173_1922-169delinsCAAAT
ENST00000463989.1:n.177-173_177-169delinsCAAAT
NM_000702.3:c.2841-173_2841-169delinsCAAAT	NP_000693.1:n.2841-173_2841-169delinsCAAAT
NM_000702.4:c.2841-173_2841-169delinsCAAAT MANE Select	NP_000693.1:n.2841-173_2841-169delinsCAAAT