Canonical Allele Identifier: CA2685126613
Gene: ATP6V0A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138706492del , CM000669.2:g.138706492del GRCh38
NC_000007.13:g.138391237del , CM000669.1:g.138391237del GRCh37
NC_000007.12:g.138041777del NCBI36
NG_008145.1:g.96706del
NG_051552.1:g.57del

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.*133del MANE Select ENSP00000308122.2:n.*133del
ENST00000478480.2:c.*221del ENSP00000495261.1:n.*221del
ENST00000644341.1:c.*133del ENSP00000495642.1:n.*133del
ENST00000645515.1:c.*133del ENSP00000496421.1:n.*133del
ENST00000647427.1:c.1431del ENSP00000496259.1:n.1431del
ENST00000310018.6:c.*133del ENSP00000308122.2:n.*133del
ENST00000393054.5:c.*133del ENSP00000376774.1:n.*133del
NM_020632.2:c.*133del NP_065683.2:n.*133del
NM_130840.2:c.*133del NP_570855.2:n.*133del
NM_130841.2:c.*133del NP_570856.2:n.*133del
XM_005250393.1:c.*133del XP_005250450.1:n.*133del
XM_005250394.2:c.*133del XP_005250451.1:n.*133del
XM_005250394.3:c.*133del XP_005250451.1:n.*133del
NM_020632.3:c.*133del MANE Select NP_065683.2:n.*133del
NM_130840.3:c.*133del NP_570855.2:n.*133del
NM_130841.3:c.*133del NP_570856.2:n.*133del