Canonical Allele Identifier: CA2839860769

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139631G>T , CM000663.2:g.160139631G>T	GRCh38
NC_000001.10:g.160109421G>T , CM000663.1:g.160109421G>T	GRCh37
NC_000001.9:g.158376045G>T	NCBI36
NG_008014.1:g.28874G>T , LRG_6:g.28874G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.2841-9G>T MANE Select	ENSP00000354490.3:n.2841-9G>T
ENST00000361216.7:c.2841-9G>T	ENSP00000354490.3:n.2841-9G>T
ENST00000392233.7:c.2841-9G>T	ENSP00000376066.3:n.2841-9G>T
ENST00000447527.1:c.1922-9G>T
ENST00000463989.1:n.177-9G>T
NM_000702.3:c.2841-9G>T	NP_000693.1:n.2841-9G>T
NM_000702.4:c.2841-9G>T MANE Select	NP_000693.1:n.2841-9G>T