Canonical Allele Identifier: CA2069005387

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744669A= , CM000674.2:g.123744669A=	GRCh38
NC_000012.11:g.124229216A= , CM000674.1:g.124229216A=	GRCh37
NC_000012.10:g.122795169A=	NCBI36
NG_012743.1:g.37352A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1399A= MANE Select	ENSP00000332247.2:p.Ile467=
ENST00000540368.6:n.1430A=
ENST00000674794.1:c.1487A=
ENST00000675260.1:n.674A=
ENST00000675344.1:c.*420A=	ENSP00000501953.1:n.*420A=
ENST00000330342.7:c.1399A=	ENSP00000332247.2:p.Ile467=
ENST00000536426.1:n.416A=
ENST00000545059.5:n.4035A=
NM_012463.3:c.1399A=	NP_036595.2:p.Ile467=
XM_005253563.1:c.1399A=	XP_005253620.1:p.Ile467=
XM_006719317.2:c.886A=	XP_006719380.1:p.Ile296=
XM_006719318.2:c.577A=	XP_006719381.1:p.Ile193=
XR_429088.1:n.1562A=
XM_024448910.1:c.1399A=	XP_024304678.1:p.Ile467=
XM_024448911.1:c.886A=	XP_024304679.1:p.Ile296=
XM_024448912.1:c.577A=	XP_024304680.1:p.Ile193=
NM_012463.4:c.1399A= MANE Select	NP_036595.2:p.Ile467=