Canonical Allele Identifier: CA1746765447

Gene: ATP6V0A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138709641G= , CM000669.2:g.138709641G=	GRCh38
NC_000007.13:g.138394386G= , CM000669.1:g.138394386G=	GRCh37
NC_000007.12:g.138044926G=	NCBI36
NG_008145.1:g.93556C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310018.7:c.2412C= MANE Select	ENSP00000308122.2:p.His804=
ENST00000478480.2:c.1366-2924C=	ENSP00000495261.1:n.1366-2924C=
ENST00000644341.1:c.1638C=	ENSP00000495642.1:p.His546=
ENST00000645515.1:c.2412C=	ENSP00000496421.1:p.His804=
ENST00000647427.1:c.1187C=	ENSP00000496259.1:n.1187C=
ENST00000310018.6:c.2412C=	ENSP00000308122.2:p.His804=
ENST00000353492.4:c.2412C=	ENSP00000253856.6:p.His804=
ENST00000393054.5:c.2412C=	ENSP00000376774.1:p.His804=
NM_020632.2:c.2412C=	NP_065683.2:p.His804=
NM_130840.2:c.2412C=	NP_570855.2:p.His804=
NM_130841.2:c.2412C=	NP_570856.2:p.His804=
XM_005250393.1:c.2412C=	XP_005250450.1:p.His804=
XM_005250394.2:c.2412C=	XP_005250451.1:p.His804=
XM_005250394.3:c.2412C=	XP_005250451.1:p.His804=
NM_020632.3:c.2412C= MANE Select	NP_065683.2:p.His804=
NM_130840.3:c.2412C=	NP_570855.2:p.His804=
NM_130841.3:c.2412C=	NP_570856.2:p.His804=