Canonical Allele Identifier: CA1746763191
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138706636T= , CM000669.2:g.138706636T= GRCh38
NC_000007.13:g.138391381T= , CM000669.1:g.138391381T= GRCh37
NC_000007.12:g.138041921T= NCBI36
NG_008145.1:g.96561A=

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.2511A= MANE Select ENSP00000308122.2:p.Thr837=
ENST00000478480.2:c.*76A= ENSP00000495261.1:n.*76A=
ENST00000644341.1:c.1737A= ENSP00000495642.1:p.Thr579=
ENST00000645515.1:c.2511A= ENSP00000496421.1:p.Thr837=
ENST00000647427.1:c.1286A= ENSP00000496259.1:n.1286A=
ENST00000310018.6:c.2511A= ENSP00000308122.2:p.Thr837=
ENST00000353492.4:c.2511A= ENSP00000253856.6:p.Thr837=
ENST00000393054.5:c.2511A= ENSP00000376774.1:p.Thr837=
NM_020632.2:c.2511A= NP_065683.2:p.Thr837=
NM_130840.2:c.2511A= NP_570855.2:p.Thr837=
NM_130841.2:c.2511A= NP_570856.2:p.Thr837=
XM_005250393.1:c.2511A= XP_005250450.1:p.Thr837=
XM_005250394.2:c.2511A= XP_005250451.1:p.Thr837=
XM_005250394.3:c.2511A= XP_005250451.1:p.Thr837=
NM_020632.3:c.2511A= MANE Select NP_065683.2:p.Thr837=
NM_130840.3:c.2511A= NP_570855.2:p.Thr837=
NM_130841.3:c.2511A= NP_570856.2:p.Thr837=