Canonical Allele Identifier: CA343256219
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160109711T>A (hg19) chr1:g.160139921T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139921T>A , CM000663.2:g.160139921T>A GRCh38
NC_000001.10:g.160109711T>A , CM000663.1:g.160109711T>A GRCh37
NC_000001.9:g.158376335T>A NCBI36
NG_008014.1:g.29164T>A , LRG_6:g.29164T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.2971T>A MANE Select ENSP00000354490.3:p.Tyr991Asn
ENST00000361216.7:c.2971T>A ENSP00000354490.3:p.Tyr991Asn
ENST00000392233.7:c.2943-5T>A ENSP00000376066.3:n.2943-5T>A
ENST00000447527.1:c.2052T>A
ENST00000463989.1:n.307T>A
NM_000702.3:c.2971T>A NP_000693.1:p.Tyr991Asn
NM_000702.4:c.2971T>A MANE Select NP_000693.1:p.Tyr991Asn
Search 100 bp 5'
Search 100 bp 3'