Canonical Allele Identifier: CA167113251
Gene: ATP6V0A4 HGNC NCBI

Linked Data

dbSNP Id: rs770369261

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138706602C>T , CM000669.2:g.138706602C>T GRCh38
NC_000007.13:g.138391347C>T , CM000669.1:g.138391347C>T GRCh37
NC_000007.12:g.138041887C>T NCBI36
NG_008145.1:g.96595G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.*22G>A MANE Select ENSP00000308122.2:n.*22G>A
ENST00000478480.2:c.*110G>A ENSP00000495261.1:n.*110G>A
ENST00000644341.1:c.*22G>A ENSP00000495642.1:n.*22G>A
ENST00000645515.1:c.*22G>A ENSP00000496421.1:n.*22G>A
ENST00000647427.1:c.1320G>A ENSP00000496259.1:n.1320G>A
ENST00000310018.6:c.*22G>A ENSP00000308122.2:n.*22G>A
ENST00000353492.4:c.*22G>A ENSP00000253856.6:n.*22G>A
ENST00000393054.5:c.*22G>A ENSP00000376774.1:n.*22G>A
NM_020632.2:c.*22G>A NP_065683.2:n.*22G>A
NM_130840.2:c.*22G>A NP_570855.2:n.*22G>A
NM_130841.2:c.*22G>A NP_570856.2:n.*22G>A
XM_005250393.1:c.*22G>A XP_005250450.1:n.*22G>A
XM_005250394.2:c.*22G>A XP_005250451.1:n.*22G>A
XM_005250394.3:c.*22G>A XP_005250451.1:n.*22G>A
NM_020632.3:c.*22G>A MANE Select NP_065683.2:n.*22G>A
NM_130840.3:c.*22G>A NP_570855.2:n.*22G>A
NM_130841.3:c.*22G>A NP_570856.2:n.*22G>A