Canonical Allele Identifier: CA882382660

Gene: ATP1A3

Linked Data

• dbSNP Id: rs1491542928
• gnomAD v3: 19-41970627-T-TC
• gnomAD v4: 19-41970627-T-TC
• MyVariant Identifiers: chr19:g.41970627_41970628insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41970627_41970628insC , CM000681.2:g.41970627_41970628insC	GRCh38
NC_000019.9:g.42474779_42474780insC , CM000681.1:g.42474779_42474780insC	GRCh37
NC_000019.8:g.47166619_47166620insC	NCBI36
NG_008015.1:g.28603_28604insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.2303-86_2303-85insG	ENSP00000444688.1:n.2303-86_2303-85insG
ENST00000644613.1:c.2264-86_2264-85insG	ENSP00000494711.1:n.2264-86_2264-85insG
ENST00000648268.1:c.2264-86_2264-85insG MANE Select	ENSP00000498113.1:n.2264-86_2264-85insG
ENST00000302102.9:c.2264-86_2264-85insG	ENSP00000302397.5:n.2264-86_2264-85insG
ENST00000441343.5:c.2264-86_2264-85insG	ENSP00000411503.1:n.2264-86_2264-85insG
ENST00000543770.5:c.2297-86_2297-85insG	ENSP00000437577.1:n.2297-86_2297-85insG
ENST00000545399.5:c.2303-86_2303-85insG	ENSP00000444688.1:n.2303-86_2303-85insG
ENST00000602133.5:c.2174-86_2174-85insG	ENSP00000471581.1:n.2174-86_2174-85insG
NM_001256213.1:c.2297-86_2297-85insG	NP_001243142.1:n.2297-86_2297-85insG
NM_001256214.1:c.2303-86_2303-85insG	NP_001243143.1:n.2303-86_2303-85insG
NM_152296.4:c.2264-86_2264-85insG	NP_689509.1:n.2264-86_2264-85insG
XM_011526991.1:c.2174-86_2174-85insG	XP_011525293.1:n.2174-86_2174-85insG
NM_152296.5:c.2264-86_2264-85insG MANE Select	NP_689509.1:n.2264-86_2264-85insG
NM_001256214.2:c.2303-86_2303-85insG	NP_001243143.1:n.2303-86_2303-85insG
NM_001256213.2:c.2297-86_2297-85insG	NP_001243142.1:n.2297-86_2297-85insG