Canonical Allele Identifier: CA1202192285
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160128784A= , CM000663.2:g.160128784A= GRCh38
NC_000001.10:g.160098574A= , CM000663.1:g.160098574A= GRCh37
NC_000001.9:g.158365198A= NCBI36
NG_008014.1:g.18027A= , LRG_6:g.18027A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1150A= MANE Select ENSP00000354490.3:p.Met384=
ENST00000361216.7:c.1150A= ENSP00000354490.3:p.Met384=
ENST00000392233.7:c.1150A= ENSP00000376066.3:p.Met384=
ENST00000447527.1:c.282A=
ENST00000472488.5:n.1253A=
NM_000702.3:c.1150A= NP_000693.1:p.Met384=
NM_000702.4:c.1150A= MANE Select NP_000693.1:p.Met384=