Canonical Allele Identifier: CA457940724

Gene: ATP6V0A4

Linked Data

• gnomAD v4: 7-138706714-A-C
• MyVariant Identifiers: chr7:g.138391459A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138706714A>C , CM000669.2:g.138706714A>C	GRCh38
NC_000007.13:g.138391459A>C , CM000669.1:g.138391459A>C	GRCh37
NC_000007.12:g.138041999A>C	NCBI36
NG_008145.1:g.96483T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310018.7:c.2433T>G MANE Select	ENSP00000308122.2:p.Val811=
ENST00000478480.2:c.1369T>G	ENSP00000495261.1:p.Ter457Gly
ENST00000644341.1:c.1659T>G	ENSP00000495642.1:p.Val553=
ENST00000645515.1:c.2433T>G	ENSP00000496421.1:p.Val811=
ENST00000647427.1:c.1208T>G	ENSP00000496259.1:n.1208T>G
ENST00000310018.6:c.2433T>G	ENSP00000308122.2:p.Val811=
ENST00000353492.4:c.2433T>G	ENSP00000253856.6:p.Val811=
ENST00000393054.5:c.2433T>G	ENSP00000376774.1:p.Val811=
NM_020632.2:c.2433T>G	NP_065683.2:p.Val811=
NM_130840.2:c.2433T>G	NP_570855.2:p.Val811=
NM_130841.2:c.2433T>G	NP_570856.2:p.Val811=
XM_005250393.1:c.2433T>G	XP_005250450.1:p.Val811=
XM_005250394.2:c.2433T>G	XP_005250451.1:p.Val811=
XM_005250394.3:c.2433T>G	XP_005250451.1:p.Val811=
NM_020632.3:c.2433T>G MANE Select	NP_065683.2:p.Val811=
NM_130840.3:c.2433T>G	NP_570855.2:p.Val811=
NM_130841.3:c.2433T>G	NP_570856.2:p.Val811=