Canonical Allele Identifier: CA2069005378

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744662T= , CM000674.2:g.123744662T=	GRCh38
NC_000012.11:g.124229209T= , CM000674.1:g.124229209T=	GRCh37
NC_000012.10:g.122795162T=	NCBI36
NG_012743.1:g.37345T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1392T= MANE Select	ENSP00000332247.2:p.Thr464=
ENST00000540368.6:n.1423T=
ENST00000674794.1:c.1480T=
ENST00000675260.1:n.667T=
ENST00000675344.1:c.*413T=	ENSP00000501953.1:n.*413T=
ENST00000330342.7:c.1392T=	ENSP00000332247.2:p.Thr464=
ENST00000536426.1:n.409T=
ENST00000545059.5:n.4028T=
NM_012463.3:c.1392T=	NP_036595.2:p.Thr464=
XM_005253563.1:c.1392T=	XP_005253620.1:p.Thr464=
XM_006719317.2:c.879T=	XP_006719380.1:p.Thr293=
XM_006719318.2:c.570T=	XP_006719381.1:p.Thr190=
XR_429088.1:n.1555T=
XM_024448910.1:c.1392T=	XP_024304678.1:p.Thr464=
XM_024448911.1:c.879T=	XP_024304679.1:p.Thr293=
XM_024448912.1:c.570T=	XP_024304680.1:p.Thr190=
NM_012463.4:c.1392T= MANE Select	NP_036595.2:p.Thr464=