Canonical Allele Identifier: CA457938023
Gene: ATP6V0A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.138424291A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138739546A>T , CM000669.2:g.138739546A>T GRCh38
NC_000007.13:g.138424291A>T , CM000669.1:g.138424291A>T GRCh37
NC_000007.12:g.138074831A>T NCBI36
NG_008145.1:g.63651T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.1566T>A MANE Select ENSP00000308122.2:p.Ile522=
ENST00000478480.2:c.792T>A ENSP00000495261.1:p.Ile264=
ENST00000644341.1:c.792T>A ENSP00000495642.1:p.Ile264=
ENST00000645515.1:c.1566T>A ENSP00000496421.1:p.Ile522=
ENST00000647427.1:n.459T>A ENSP00000496259.1:p.Ile153=
ENST00000310018.6:c.1566T>A ENSP00000308122.2:p.Ile522=
ENST00000353492.4:c.1566T>A ENSP00000253856.6:p.Ile522=
ENST00000393054.5:c.1566T>A ENSP00000376774.1:p.Ile522=
ENST00000471085.1:n.252-5292T>A
NM_020632.2:c.1566T>A NP_065683.2:p.Ile522=
NM_130840.2:c.1566T>A NP_570855.2:p.Ile522=
NM_130841.2:c.1566T>A NP_570856.2:p.Ile522=
XM_005250393.1:c.1566T>A XP_005250450.1:p.Ile522=
XM_005250394.2:c.1566T>A XP_005250451.1:p.Ile522=
XM_005250394.3:c.1566T>A XP_005250451.1:p.Ile522=
NM_020632.3:c.1566T>A MANE Select NP_065683.2:p.Ile522=
NM_130840.3:c.1566T>A NP_570855.2:p.Ile522=
NM_130841.3:c.1566T>A NP_570856.2:p.Ile522=