Canonical Allele Identifier: CA406052166
Gene: ATP1A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 427061
ClinVar RCV Id: RCV000489150 RCV000703309
dbSNP Id: rs1085307933
MyVariant Identifiers: chr19:g.42489095G>A (hg19) chr19:g.41984943G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41984943G>A , CM000681.2:g.41984943G>A GRCh38
NC_000019.9:g.42489095G>A , CM000681.1:g.42489095G>A GRCh37
NC_000019.8:g.47180935G>A NCBI36
NG_008015.1:g.14288C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000545399.6:c.1007C>T ENSP00000444688.1:p.Pro336Leu
ENST00000644613.1:c.968C>T ENSP00000494711.1:p.Pro323Leu
ENST00000648268.1:c.968C>T MANE Select ENSP00000498113.1:p.Pro323Leu
ENST00000302102.9:c.968C>T ENSP00000302397.5:p.Pro323Leu
ENST00000441343.5:c.968C>T ENSP00000411503.1:p.Pro323Leu
ENST00000485672.2:n.281C>T
ENST00000543770.5:c.1001C>T ENSP00000437577.1:p.Pro334Leu
ENST00000545399.5:c.1007C>T ENSP00000444688.1:p.Pro336Leu
ENST00000602133.5:c.878C>T ENSP00000471581.1:p.Pro293Leu
NM_001256213.1:c.1001C>T NP_001243142.1:p.Pro334Leu
NM_001256214.1:c.1007C>T NP_001243143.1:p.Pro336Leu
NM_152296.4:c.968C>T NP_689509.1:p.Pro323Leu
XM_011526991.1:c.878C>T XP_011525293.1:p.Pro293Leu
NM_152296.5:c.968C>T MANE Select NP_689509.1:p.Pro323Leu
NM_001256214.2:c.1007C>T NP_001243143.1:p.Pro336Leu
NM_001256213.2:c.1001C>T NP_001243142.1:p.Pro334Leu
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