Canonical Allele Identifier: CA507695098

Gene: ATP1A3

Linked Data

• MyVariant Identifiers: chr19:g.42486193A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41982041A>C , CM000681.2:g.41982041A>C	GRCh38
NC_000019.9:g.42486193A>C , CM000681.1:g.42486193A>C	GRCh37
NC_000019.8:g.47178033A>C	NCBI36
NG_008015.1:g.17190T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.1098T>G	ENSP00000444688.1:p.Ala366=
ENST00000644613.1:c.1059T>G	ENSP00000494711.1:p.Ala353=
ENST00000648268.1:c.1059T>G MANE Select	ENSP00000498113.1:p.Ala353=
ENST00000302102.9:c.1059T>G	ENSP00000302397.5:p.Ala353=
ENST00000441343.5:c.1059T>G	ENSP00000411503.1:p.Ala353=
ENST00000543770.5:c.1092T>G	ENSP00000437577.1:p.Ala364=
ENST00000545399.5:c.1098T>G	ENSP00000444688.1:p.Ala366=
ENST00000602133.5:c.969T>G	ENSP00000471581.1:p.Ala323=
NM_001256213.1:c.1092T>G	NP_001243142.1:p.Ala364=
NM_001256214.1:c.1098T>G	NP_001243143.1:p.Ala366=
NM_152296.4:c.1059T>G	NP_689509.1:p.Ala353=
XM_011526991.1:c.969T>G	XP_011525293.1:p.Ala323=
NM_152296.5:c.1059T>G MANE Select	NP_689509.1:p.Ala353=
NM_001256214.2:c.1098T>G	NP_001243143.1:p.Ala366=
NM_001256213.2:c.1092T>G	NP_001243142.1:p.Ala364=