Canonical Allele Identifier: CA2842419297
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138739547dup , CM000669.2:g.138739547dup GRCh38
NC_000007.13:g.138424292dup , CM000669.1:g.138424292dup GRCh37
NC_000007.12:g.138074832dup NCBI36
NG_008145.1:g.63651dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000310018.7:c.1566dup MANE Select ENSP00000308122.2:p.Asp523Ter
ENST00000478480.2:c.792dup ENSP00000495261.1:p.Asp265Ter
ENST00000644341.1:c.792dup ENSP00000495642.1:p.Asp265Ter
ENST00000645515.1:c.1566dup ENSP00000496421.1:p.Asp523Ter
ENST00000647427.1:c.459dup ENSP00000496259.1:p.Asp154Ter
ENST00000310018.6:c.1566dup ENSP00000308122.2:p.Asp523Ter
ENST00000353492.4:c.1566dup ENSP00000253856.6:p.Asp523Ter
ENST00000393054.5:c.1566dup ENSP00000376774.1:p.Asp523Ter
ENST00000471085.1:n.252-5292dup
NM_020632.2:c.1566dup NP_065683.2:p.Asp523Ter
NM_130840.2:c.1566dup NP_570855.2:p.Asp523Ter
NM_130841.2:c.1566dup NP_570856.2:p.Asp523Ter
XM_005250393.1:c.1566dup XP_005250450.1:p.Asp523Ter
XM_005250394.2:c.1566dup XP_005250451.1:p.Asp523Ter
XM_005250394.3:c.1566dup XP_005250451.1:p.Asp523Ter
NM_020632.3:c.1566dup MANE Select NP_065683.2:p.Asp523Ter
NM_130840.3:c.1566dup NP_570855.2:p.Asp523Ter
NM_130841.3:c.1566dup NP_570856.2:p.Asp523Ter