Canonical Allele Identifier: CA9467335
Community Standard Title: NM_152296.5(ATP1A3):c.2616C>A (p.Asn872Lys)
Gene: ATP1A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41969507G>T , CM000681.2:g.41969507G>T GRCh38
NC_000019.9:g.42473659G>T , CM000681.1:g.42473659G>T GRCh37
NC_000019.8:g.47165499G>T NCBI36
NG_008015.1:g.29724C>A

Transcript Alleles

HGVS Amino-acid Change
NM_152296.5:c.2616C>A MANE Select NP_689509.1:p.Asn872Lys
ENST00000648268.1:c.2616C>A MANE Select ENSP00000498113.1:p.Asn872Lys
NM_001256213.1:c.2649C>A NP_001243142.1:p.Asn883Lys
NM_001256213.2:c.2649C>A NP_001243142.1:p.Asn883Lys
NM_001256214.1:c.2655C>A NP_001243143.1:p.Asn885Lys
NM_001256214.2:c.2655C>A NP_001243143.1:p.Asn885Lys
NM_152296.4:c.2616C>A NP_689509.1:p.Asn872Lys
ENST00000302102.9:c.2616C>A ENSP00000302397.5:p.Asn872Lys
ENST00000441343.5:c.2616C>A ENSP00000411503.1:p.Asn872Lys
ENST00000543770.5:c.2649C>A ENSP00000437577.1:p.Asn883Lys
ENST00000545399.5:c.2655C>A ENSP00000444688.1:p.Asn885Lys
ENST00000545399.6:c.2655C>A ENSP00000444688.1:p.Asn885Lys
ENST00000602133.5:c.2526C>A ENSP00000471581.1:p.Asn842Lys
ENST00000644613.1:c.2616C>A ENSP00000494711.1:p.Asn872Lys
XM_011526991.1:c.2526C>A XP_011525293.1:p.Asn842Lys