Canonical Allele Identifier: CA1202192915

Gene: ATP1A2

Linked Data

• dbSNP Id: rs1651732147

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130302del , CM000663.2:g.160130302del	GRCh38
NC_000001.10:g.160100092del , CM000663.1:g.160100092del	GRCh37
NC_000001.9:g.158366716del	NCBI36
NG_008014.1:g.19545del , LRG_6:g.19545del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361216.8:c.1651+11del MANE Select	ENSP00000354490.3:n.1651+11del
ENST00000361216.7:c.1651+11del	ENSP00000354490.3:n.1651+11del
ENST00000392233.7:c.1651+11del	ENSP00000376066.3:n.1651+11del
ENST00000447527.1:c.783+11del
ENST00000472488.5:n.1754+11del
NM_000702.3:c.1651+11del	NP_000693.1:n.1651+11del
NM_000702.4:c.1651+11del MANE Select	NP_000693.1:n.1651+11del