Canonical Allele Identifier: CA918143632

Gene: ATP6V0A4

Linked Data

• dbSNP Id: rs1584907511

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138732799_138732800insG , CM000669.2:g.138732799_138732800insG	GRCh38
NC_000007.13:g.138417544_138417545insG , CM000669.1:g.138417544_138417545insG	GRCh37
NC_000007.12:g.138068084_138068085insG	NCBI36
NG_008145.1:g.70397_70398insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.1908+77_1908+78insC MANE Select	ENSP00000308122.2:n.1908+77_1908+78insC
ENST00000478480.2:c.1134+77_1134+78insC	ENSP00000495261.1:n.1134+77_1134+78insC
ENST00000644341.1:c.1134+77_1134+78insC	ENSP00000495642.1:n.1134+77_1134+78insC
ENST00000645515.1:c.1908+77_1908+78insC	ENSP00000496421.1:n.1908+77_1908+78insC
ENST00000647427.1:c.801+77_801+78insC	ENSP00000496259.1:n.801+77_801+78insC
ENST00000310018.6:c.1908+77_1908+78insC	ENSP00000308122.2:n.1908+77_1908+78insC
ENST00000353492.4:c.1908+77_1908+78insC	ENSP00000253856.6:n.1908+77_1908+78insC
ENST00000393054.5:c.1908+77_1908+78insC	ENSP00000376774.1:n.1908+77_1908+78insC
NM_020632.2:c.1908+77_1908+78insC	NP_065683.2:n.1908+77_1908+78insC
NM_130840.2:c.1908+77_1908+78insC	NP_570855.2:n.1908+77_1908+78insC
NM_130841.2:c.1908+77_1908+78insC	NP_570856.2:n.1908+77_1908+78insC
XM_005250393.1:c.1908+77_1908+78insC	XP_005250450.1:n.1908+77_1908+78insC
XM_005250394.2:c.1908+77_1908+78insC	XP_005250451.1:n.1908+77_1908+78insC
XM_005250394.3:c.1908+77_1908+78insC	XP_005250451.1:n.1908+77_1908+78insC
NM_020632.3:c.1908+77_1908+78insC MANE Select	NP_065683.2:n.1908+77_1908+78insC
NM_130840.3:c.1908+77_1908+78insC	NP_570855.2:n.1908+77_1908+78insC
NM_130841.3:c.1908+77_1908+78insC	NP_570856.2:n.1908+77_1908+78insC