Canonical Allele Identifier: CA406039502

Gene: ATP1A3

Linked Data

• MyVariant Identifiers: chr19:g.42474611A>T (hg19) ; chr19:g.41970459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41970459A>T , CM000681.2:g.41970459A>T	GRCh38
NC_000019.9:g.42474611A>T , CM000681.1:g.42474611A>T	GRCh37
NC_000019.8:g.47166451A>T	NCBI36
NG_008015.1:g.28772T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.2386T>A	ENSP00000444688.1:p.Phe796Ile
ENST00000644613.1:c.2347T>A	ENSP00000494711.1:p.Phe783Ile
ENST00000648268.1:c.2347T>A MANE Select	ENSP00000498113.1:p.Phe783Ile
ENST00000302102.9:c.2347T>A	ENSP00000302397.5:p.Phe783Ile
ENST00000441343.5:c.2347T>A	ENSP00000411503.1:p.Phe783Ile
ENST00000543770.5:c.2380T>A	ENSP00000437577.1:p.Phe794Ile
ENST00000545399.5:c.2386T>A	ENSP00000444688.1:p.Phe796Ile
ENST00000602133.5:c.2257T>A	ENSP00000471581.1:p.Phe753Ile
NM_001256213.1:c.2380T>A	NP_001243142.1:p.Phe794Ile
NM_001256214.1:c.2386T>A	NP_001243143.1:p.Phe796Ile
NM_152296.4:c.2347T>A	NP_689509.1:p.Phe783Ile
XM_011526991.1:c.2257T>A	XP_011525293.1:p.Phe753Ile
NM_152296.5:c.2347T>A MANE Select	NP_689509.1:p.Phe783Ile
NM_001256214.2:c.2386T>A	NP_001243143.1:p.Phe796Ile
NM_001256213.2:c.2380T>A	NP_001243142.1:p.Phe794Ile