Canonical Allele Identifier: CA2068977403

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724765A= , CM000674.2:g.123724765A=	GRCh38
NC_000012.11:g.124209312A= , CM000674.1:g.124209312A=	GRCh37
NC_000012.10:g.122775265A=	NCBI36
NG_012743.1:g.17448A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.406A= MANE Select	ENSP00000332247.2:p.Lys136=
ENST00000540368.6:n.437A=
ENST00000613625.5:c.406A=	ENSP00000482236.1:p.Lys136=
ENST00000675344.1:c.406A=	ENSP00000501953.1:p.Lys136=
ENST00000330342.7:c.406A=	ENSP00000332247.2:p.Lys136=
ENST00000504192.2:c.16A=	ENSP00000443441.1:p.Lys6=
ENST00000540368.5:n.616A=
ENST00000613625.4:c.406A=	ENSP00000482236.1:p.Lys136=
NM_012463.3:c.406A=	NP_036595.2:p.Lys136=
XM_005253563.1:c.406A=	XP_005253620.1:p.Lys136=
XM_006719317.2:c.-19A=	XP_006719380.1:n.-19A=
XR_429088.1:n.569A=
XM_024448910.1:c.406A=	XP_024304678.1:p.Lys136=
XM_024448911.1:c.-19A=	XP_024304679.1:n.-19A=
NM_012463.4:c.406A= MANE Select	NP_036595.2:p.Lys136=