Canonical Allele Identifier: CA1746780024
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138739554A= , CM000669.2:g.138739554A= GRCh38
NC_000007.13:g.138424299A= , CM000669.1:g.138424299A= GRCh37
NC_000007.12:g.138074839A= NCBI36
NG_008145.1:g.63643T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.1558T= MANE Select ENSP00000308122.2:p.Phe520=
ENST00000478480.2:c.784T= ENSP00000495261.1:p.Phe262=
ENST00000644341.1:c.784T= ENSP00000495642.1:p.Phe262=
ENST00000645515.1:c.1558T= ENSP00000496421.1:p.Phe520=
ENST00000647427.1:n.451T= ENSP00000496259.1:p.Phe151=
ENST00000310018.6:c.1558T= ENSP00000308122.2:p.Phe520=
ENST00000353492.4:c.1558T= ENSP00000253856.6:p.Phe520=
ENST00000393054.5:c.1558T= ENSP00000376774.1:p.Phe520=
ENST00000471085.1:n.252-5300T=
NM_020632.2:c.1558T= NP_065683.2:p.Phe520=
NM_130840.2:c.1558T= NP_570855.2:p.Phe520=
NM_130841.2:c.1558T= NP_570856.2:p.Phe520=
XM_005250393.1:c.1558T= XP_005250450.1:p.Phe520=
XM_005250394.2:c.1558T= XP_005250451.1:p.Phe520=
XM_005250394.3:c.1558T= XP_005250451.1:p.Phe520=
NM_020632.3:c.1558T= MANE Select NP_065683.2:p.Phe520=
NM_130840.3:c.1558T= NP_570855.2:p.Phe520=
NM_130841.3:c.1558T= NP_570856.2:p.Phe520=