Canonical Allele Identifier: CA2069005250

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744613T= , CM000674.2:g.123744613T=	GRCh38
NC_000012.11:g.124229160T= , CM000674.1:g.124229160T=	GRCh37
NC_000012.10:g.122795113T=	NCBI36
NG_012743.1:g.37296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1343T= MANE Select	ENSP00000332247.2:p.Phe448=
ENST00000540368.6:n.1374T=
ENST00000674794.1:c.1431T=
ENST00000675260.1:n.618T=
ENST00000675344.1:c.*364T=	ENSP00000501953.1:n.*364T=
ENST00000330342.7:c.1343T=	ENSP00000332247.2:p.Phe448=
ENST00000504192.2:c.953T=	ENSP00000443441.1:p.Phe318=
ENST00000536426.1:n.360T=
ENST00000545059.5:n.3979T=
NM_012463.3:c.1343T=	NP_036595.2:p.Phe448=
XM_005253563.1:c.1343T=	XP_005253620.1:p.Phe448=
XM_006719317.2:c.830T=	XP_006719380.1:p.Phe277=
XM_006719318.2:c.521T=	XP_006719381.1:p.Phe174=
XR_429088.1:n.1506T=
XM_024448910.1:c.1343T=	XP_024304678.1:p.Phe448=
XM_024448911.1:c.830T=	XP_024304679.1:p.Phe277=
XM_024448912.1:c.521T=	XP_024304680.1:p.Phe174=
NM_012463.4:c.1343T= MANE Select	NP_036595.2:p.Phe448=