Canonical Allele Identifier: CA1746763531

Gene: ATP6V0A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138706302T= , CM000669.2:g.138706302T=	GRCh38
NC_000007.13:g.138391047T= , CM000669.1:g.138391047T=	GRCh37
NC_000007.12:g.138041587T=	NCBI36
NG_008145.1:g.96895A=
NG_051552.1:g.246A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.*322A= MANE Select	ENSP00000308122.2:n.*322A=
ENST00000645515.1:c.*322A=	ENSP00000496421.1:n.*322A=
ENST00000310018.6:c.*322A=	ENSP00000308122.2:n.*322A=
ENST00000393054.5:c.*322A=	ENSP00000376774.1:n.*322A=
NM_020632.2:c.*322A=	NP_065683.2:n.*322A=
NM_130840.2:c.*322A=	NP_570855.2:n.*322A=
NM_130841.2:c.*322A=	NP_570856.2:n.*322A=
XM_005250393.1:c.*322A=	XP_005250450.1:n.*322A=
XM_005250394.2:c.*322A=	XP_005250451.1:n.*322A=
XM_005250394.3:c.*322A=	XP_005250451.1:n.*322A=
NM_020632.3:c.*322A= MANE Select	NP_065683.2:n.*322A=
NM_130840.3:c.*322A=	NP_570855.2:n.*322A=
NM_130841.3:c.*322A=	NP_570856.2:n.*322A=