Canonical Allele Identifier: CA1025542
Gene: ATP1A1 HGNC NCBI
ATP1A1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.116399109C>G , CM000663.2:g.116399109C>G GRCh38
NC_000001.10:g.116941731C>G , CM000663.1:g.116941731C>G GRCh37
NC_000001.9:g.116743254C>G NCBI36
NG_047036.1:g.31925C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000701.8:c.2448+25C>G (ATP1A1) MANE Select NP_000692.2:n.2448+25C>G
ENST00000295598.10:c.2448+25C>G (ATP1A1) MANE Select ENSP00000295598.5:n.2448+25C>G
NM_000701.7:c.2448+25C>G (ATP1A1) NP_000692.2:n.2448+25C>G
NM_001160233.1:c.2448+25C>G (ATP1A1) NP_001153705.1:n.2448+25C>G
NM_001160233.2:c.2448+25C>G (ATP1A1) NP_001153705.1:n.2448+25C>G
NM_001160234.1:c.2355+25C>G (ATP1A1) NP_001153706.1:n.2355+25C>G
NM_001160234.2:c.2355+25C>G (ATP1A1) NP_001153706.1:n.2355+25C>G
NR_027645.1:n.559G>C (ATP1A1-AS1)
NR_027646.1:n.400+1787G>C (ATP1A1-AS1)
ENST00000295598.9:c.2448+25C>G (ATP1A1) ENSP00000295598.5:n.2448+25C>G
ENST00000369496.8:c.2355+25C>G (ATP1A1) ENSP00000358508.4:n.2355+25C>G
ENST00000537345.5:c.2448+25C>G (ATP1A1) ENSP00000445306.1:n.2448+25C>G
XM_006710655.2:c.2355+25C>G (ATP1A1) XP_006710718.1:n.2355+25C>G
XM_017001360.1:c.2355+25C>G (ATP1A1) XP_016856849.1:n.2355+25C>G
XM_017001361.1:c.2355+25C>G (ATP1A1) XP_016856850.1:n.2355+25C>G
XR_002956654.1:n.2974+25C>G (ATP1A1)