Canonical Allele Identifier: CA434945510
Community Standard Title: NM_001690.4(ATP6V1A):c.354C>A (p.Ile118=)
Gene: ATP6V1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.113784366C>A , CM000665.2:g.113784366C>A GRCh38
NC_000003.11:g.113503213C>A , CM000665.1:g.113503213C>A GRCh37
NC_000003.10:g.114985903C>A NCBI36
NG_047012.1:g.42348C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001690.4:c.354C>A MANE Select NP_001681.2:p.Ile118=
ENST00000273398.8:c.354C>A MANE Select ENSP00000273398.3:p.Ile118=
NM_001690.3:c.354C>A NP_001681.2:p.Ile118=
ENST00000273398.7:c.354C>A ENSP00000273398.3:p.Ile118=
ENST00000470455.5:c.*256C>A ENSP00000420146.1:n.*256C>A
ENST00000475322.1:c.354C>A ENSP00000419294.1:p.Ile118=
ENST00000496747.5:c.255C>A ENSP00000417545.1:p.Ile85=
ENST00000496747.6:c.255C>A ENSP00000417545.2:p.Ile85=
ENST00000703904.2:c.354C>A ENSP00000515542.1:p.Ile118=
ENST00000703907.1:n.454C>A
ENST00000703908.1:c.354C>A ENSP00000515545.1:p.Ile118=
ENST00000703909.1:c.354C>A ENSP00000515546.1:p.Ile118=
ENST00000703910.1:c.354C>A ENSP00000515547.1:p.Ile118=
ENST00000703911.1:c.354C>A ENSP00000515548.1:p.Ile118=