Canonical Allele Identifier: CA1746790656
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138763003C= , CM000669.2:g.138763003C= GRCh38
NC_000007.13:g.138447748C= , CM000669.1:g.138447748C= GRCh37
NC_000007.12:g.138098288C= NCBI36
NG_008145.1:g.40194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310018.7:c.314G= MANE Select ENSP00000308122.2:p.Gly105=
ENST00000645515.1:c.314G= ENSP00000496421.1:p.Gly105=
ENST00000310018.6:c.314G= ENSP00000308122.2:p.Gly105=
ENST00000353492.4:c.314G= ENSP00000253856.6:p.Gly105=
ENST00000393054.5:c.314G= ENSP00000376774.1:p.Gly105=
ENST00000483139.1:n.563G=
NM_020632.2:c.314G= NP_065683.2:p.Gly105=
NM_130840.2:c.314G= NP_570855.2:p.Gly105=
NM_130841.2:c.314G= NP_570856.2:p.Gly105=
XM_005250393.1:c.314G= XP_005250450.1:p.Gly105=
XM_005250394.2:c.314G= XP_005250451.1:p.Gly105=
XM_005250394.3:c.314G= XP_005250451.1:p.Gly105=
NM_020632.3:c.314G= MANE Select NP_065683.2:p.Gly105=
NM_130840.3:c.314G= NP_570855.2:p.Gly105=
NM_130841.3:c.314G= NP_570856.2:p.Gly105=