Canonical Allele Identifier: CA507694753

Gene: ATP1A3

Linked Data

• gnomAD v4: 19-41970288-C-G
• MyVariant Identifiers: chr19:g.42474440C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41970288C>G , CM000681.2:g.41970288C>G	GRCh38
NC_000019.9:g.42474440C>G , CM000681.1:g.42474440C>G	GRCh37
NC_000019.8:g.47166280C>G	NCBI36
NG_008015.1:g.28943G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000545399.6:c.2478G>C	ENSP00000444688.1:p.Ala826=
ENST00000644613.1:c.2439G>C	ENSP00000494711.1:p.Ala813=
ENST00000648268.1:c.2439G>C MANE Select	ENSP00000498113.1:p.Ala813=
ENST00000302102.9:c.2439G>C	ENSP00000302397.5:p.Ala813=
ENST00000441343.5:c.2439G>C	ENSP00000411503.1:p.Ala813=
ENST00000543770.5:c.2472G>C	ENSP00000437577.1:p.Ala824=
ENST00000545399.5:c.2478G>C	ENSP00000444688.1:p.Ala826=
ENST00000602133.5:c.2349G>C	ENSP00000471581.1:p.Ala783=
NM_001256213.1:c.2472G>C	NP_001243142.1:p.Ala824=
NM_001256214.1:c.2478G>C	NP_001243143.1:p.Ala826=
NM_152296.4:c.2439G>C	NP_689509.1:p.Ala813=
XM_011526991.1:c.2349G>C	XP_011525293.1:p.Ala783=
NM_152296.5:c.2439G>C MANE Select	NP_689509.1:p.Ala813=
NM_001256214.2:c.2478G>C	NP_001243143.1:p.Ala826=
NM_001256213.2:c.2472G>C	NP_001243142.1:p.Ala824=