Canonical Allele Identifier: CA1202196745

Gene: ATP1A2

Linked Data

• dbSNP Id: rs1652060795

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139369del , CM000663.2:g.160139369del	GRCh38
NC_000001.10:g.160109159del , CM000663.1:g.160109159del	GRCh37
NC_000001.9:g.158375783del	NCBI36
NG_008014.1:g.28612del , LRG_6:g.28612del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.2841-271del MANE Select	ENSP00000354490.3:n.2841-271del
ENST00000361216.7:c.2841-271del	ENSP00000354490.3:n.2841-271del
ENST00000392233.7:c.2841-271del	ENSP00000376066.3:n.2841-271del
ENST00000447527.1:c.1922-271del
ENST00000463989.1:n.177-271del
NM_000702.3:c.2841-271del	NP_000693.1:n.2841-271del
NM_000702.4:c.2841-271del MANE Select	NP_000693.1:n.2841-271del