Canonical Allele Identifier: CA652086363

Gene: ATP6V0A4

Linked Data

• dbSNP Id: rs762913168
• gnomAD v3: 7-138733232-AC-A
• gnomAD v4: 7-138733232-AC-A
• COSMIC: COSN18731527

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138733239del , CM000669.2:g.138733239del	GRCh38
NC_000007.13:g.138417984del , CM000669.1:g.138417984del	GRCh37
NC_000007.12:g.138068524del	NCBI36
NG_008145.1:g.69964del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.1692-140del MANE Select	ENSP00000308122.2:n.1692-140del
ENST00000478480.2:c.918-140del	ENSP00000495261.1:n.918-140del
ENST00000644341.1:c.918-140del	ENSP00000495642.1:n.918-140del
ENST00000645515.1:c.1692-140del	ENSP00000496421.1:n.1692-140del
ENST00000647427.1:c.585-140del	ENSP00000496259.1:n.585-140del
ENST00000310018.6:c.1692-140del	ENSP00000308122.2:n.1692-140del
ENST00000353492.4:c.1692-140del	ENSP00000253856.6:n.1692-140del
ENST00000393054.5:c.1692-140del	ENSP00000376774.1:n.1692-140del
NM_020632.2:c.1692-140del	NP_065683.2:n.1692-140del
NM_130840.2:c.1692-140del	NP_570855.2:n.1692-140del
NM_130841.2:c.1692-140del	NP_570856.2:n.1692-140del
XM_005250393.1:c.1692-140del	XP_005250450.1:n.1692-140del
XM_005250394.2:c.1692-140del	XP_005250451.1:n.1692-140del
XM_005250394.3:c.1692-140del	XP_005250451.1:n.1692-140del
NM_020632.3:c.1692-140del MANE Select	NP_065683.2:n.1692-140del
NM_130840.3:c.1692-140del	NP_570855.2:n.1692-140del
NM_130841.3:c.1692-140del	NP_570856.2:n.1692-140del