Canonical Allele Identifier: CA652143476

Gene: ATP6V0A4

Linked Data

• COSMIC: COSN19662697

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138706585dup , CM000669.2:g.138706585dup	GRCh38
NC_000007.13:g.138391330dup , CM000669.1:g.138391330dup	GRCh37
NC_000007.12:g.138041870dup	NCBI36
NG_008145.1:g.96612dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.*39dup MANE Select	ENSP00000308122.2:n.*39dup
ENST00000478480.2:c.*127dup	ENSP00000495261.1:n.*127dup
ENST00000644341.1:c.*39dup	ENSP00000495642.1:n.*39dup
ENST00000645515.1:c.*39dup	ENSP00000496421.1:n.*39dup
ENST00000647427.1:c.1337dup	ENSP00000496259.1:n.1337dup
ENST00000310018.6:c.*39dup	ENSP00000308122.2:n.*39dup
ENST00000353492.4:c.*39dup	ENSP00000253856.6:n.*39dup
ENST00000393054.5:c.*39dup	ENSP00000376774.1:n.*39dup
NM_020632.2:c.*39dup	NP_065683.2:n.*39dup
NM_130840.2:c.*39dup	NP_570855.2:n.*39dup
NM_130841.2:c.*39dup	NP_570856.2:n.*39dup
XM_005250393.1:c.*39dup	XP_005250450.1:n.*39dup
XM_005250394.2:c.*39dup	XP_005250451.1:n.*39dup
XM_005250394.3:c.*39dup	XP_005250451.1:n.*39dup
NM_020632.3:c.*39dup MANE Select	NP_065683.2:n.*39dup
NM_130840.3:c.*39dup	NP_570855.2:n.*39dup
NM_130841.3:c.*39dup	NP_570856.2:n.*39dup