Canonical Allele Identifier: CA343243840

Gene: ATP1A2

Linked Data

• MyVariant Identifiers: chr1:g.160100083T>G (hg19) ; chr1:g.160130293T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130293T>G , CM000663.2:g.160130293T>G	GRCh38
NC_000001.10:g.160100083T>G , CM000663.1:g.160100083T>G	GRCh37
NC_000001.9:g.158366707T>G	NCBI36
NG_008014.1:g.19536T>G , LRG_6:g.19536T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361216.8:c.1651+2T>G MANE Select	ENSP00000354490.3:n.1651+2T>G
ENST00000361216.7:c.1651+2T>G	ENSP00000354490.3:n.1651+2T>G
ENST00000392233.7:c.1651+2T>G	ENSP00000376066.3:n.1651+2T>G
ENST00000447527.1:c.783+2T>G
ENST00000472488.5:n.1754+2T>G
NM_000702.3:c.1651+2T>G	NP_000693.1:n.1651+2T>G
NM_000702.4:c.1651+2T>G MANE Select	NP_000693.1:n.1651+2T>G