Canonical Allele Identifier: CA406052388

Gene: ATP1A3

Linked Data

• MyVariant Identifiers: chr19:g.42489134G>A (hg19) ; chr19:g.41984982G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41984982G>A , CM000681.2:g.41984982G>A	GRCh38
NC_000019.9:g.42489134G>A , CM000681.1:g.42489134G>A	GRCh37
NC_000019.8:g.47180974G>A	NCBI36
NG_008015.1:g.14249C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.968C>T	ENSP00000444688.1:p.Ala323Val
ENST00000644613.1:c.929C>T	ENSP00000494711.1:p.Ala310Val
ENST00000648268.1:c.929C>T MANE Select	ENSP00000498113.1:p.Ala310Val
ENST00000302102.9:c.929C>T	ENSP00000302397.5:p.Ala310Val
ENST00000441343.5:c.929C>T	ENSP00000411503.1:p.Ala310Val
ENST00000485672.2:n.242C>T
ENST00000543770.5:c.962C>T	ENSP00000437577.1:p.Ala321Val
ENST00000545399.5:c.968C>T	ENSP00000444688.1:p.Ala323Val
ENST00000602133.5:c.839C>T	ENSP00000471581.1:p.Ala280Val
NM_001256213.1:c.962C>T	NP_001243142.1:p.Ala321Val
NM_001256214.1:c.968C>T	NP_001243143.1:p.Ala323Val
NM_152296.4:c.929C>T	NP_689509.1:p.Ala310Val
XM_011526991.1:c.839C>T	XP_011525293.1:p.Ala280Val
NM_152296.5:c.929C>T MANE Select	NP_689509.1:p.Ala310Val
NM_001256214.2:c.968C>T	NP_001243143.1:p.Ala323Val
NM_001256213.2:c.962C>T	NP_001243142.1:p.Ala321Val