Canonical Allele Identifier: CA2585371577

Gene: ATP1A3

Linked Data

• gnomAD v4: 19-41987840-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41987840G>A , CM000681.2:g.41987840G>A	GRCh38
NC_000019.9:g.42491992G>A , CM000681.1:g.42491992G>A	GRCh37
NC_000019.8:g.47183832G>A	NCBI36
NG_008015.1:g.11391C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000545399.6:c.396+96C>T	ENSP00000444688.1:n.396+96C>T
ENST00000644613.1:c.357+96C>T	ENSP00000494711.1:n.357+96C>T
ENST00000648268.1:c.357+96C>T MANE Select	ENSP00000498113.1:n.357+96C>T
ENST00000302102.9:c.357+96C>T	ENSP00000302397.5:n.357+96C>T
ENST00000441343.5:c.357+96C>T	ENSP00000411503.1:n.357+96C>T
ENST00000473086.3:c.267+96C>T	ENSP00000469129.2:n.267+96C>T
ENST00000543770.5:c.390+96C>T	ENSP00000437577.1:n.390+96C>T
ENST00000545399.5:c.396+96C>T	ENSP00000444688.1:n.396+96C>T
ENST00000602133.5:c.267+96C>T	ENSP00000471581.1:n.267+96C>T
NM_001256213.1:c.390+96C>T	NP_001243142.1:n.390+96C>T
NM_001256214.1:c.396+96C>T	NP_001243143.1:n.396+96C>T
NM_152296.4:c.357+96C>T	NP_689509.1:n.357+96C>T
XM_011526991.1:c.267+96C>T	XP_011525293.1:n.267+96C>T
NM_152296.5:c.357+96C>T MANE Select	NP_689509.1:n.357+96C>T
NM_001256214.2:c.396+96C>T	NP_001243143.1:n.396+96C>T
NM_001256213.2:c.390+96C>T	NP_001243142.1:n.390+96C>T