Canonical Allele Identifier: CA1746763727
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138706600A= , CM000669.2:g.138706600A= GRCh38
NC_000007.13:g.138391345A= , CM000669.1:g.138391345A= GRCh37
NC_000007.12:g.138041885A= NCBI36
NG_008145.1:g.96597T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.*24T= MANE Select ENSP00000308122.2:p.=
ENST00000478480.2:c.*112T= ENSP00000495261.1:p.=
ENST00000644341.1:c.*24T= ENSP00000495642.1:p.=
ENST00000645515.1:c.*24T= ENSP00000496421.1:p.=
ENST00000647427.1:n.1322T= ENSP00000496259.1:p.=
ENST00000310018.6:c.*24T= ENSP00000308122.2:p.=
ENST00000353492.4:c.*24T= ENSP00000253856.6:p.=
ENST00000393054.5:c.*24T= ENSP00000376774.1:p.=
NM_020632.2:c.*24T= NP_065683.2:p.=
NM_130840.2:c.*24T= NP_570855.2:p.=
NM_130841.2:c.*24T= NP_570856.2:p.=
XM_005250393.1:c.*24T= XP_005250450.1:p.=
XM_005250394.2:c.*24T= XP_005250451.1:p.=
XM_005250394.3:c.*24T= XP_005250451.1:p.=
NM_020632.3:c.*24T= MANE Select NP_065683.2:p.=
NM_130840.3:c.*24T= NP_570855.2:p.=
NM_130841.3:c.*24T= NP_570856.2:p.=