Canonical Allele Identifier: CA2069003811

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743861C= , CM000674.2:g.123743861C=	GRCh38
NC_000012.11:g.124228408C= , CM000674.1:g.124228408C=	GRCh37
NC_000012.10:g.122794361C=	NCBI36
NG_012743.1:g.36544C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1115C= MANE Select	ENSP00000332247.2:p.Thr372=
ENST00000540368.6:n.1146C=
ENST00000674794.1:c.1203C=
ENST00000675260.1:n.390C=
ENST00000675344.1:c.*136C=	ENSP00000501953.1:n.*136C=
ENST00000330342.7:c.1115C=	ENSP00000332247.2:p.Thr372=
ENST00000504192.2:c.725C=	ENSP00000443441.1:p.Thr242=
ENST00000536426.1:n.132C=
ENST00000545059.5:n.3751C=
NM_012463.3:c.1115C=	NP_036595.2:p.Thr372=
XM_005253563.1:c.1115C=	XP_005253620.1:p.Thr372=
XM_006719317.2:c.602C=	XP_006719380.1:p.Thr201=
XM_006719318.2:c.293C=	XP_006719381.1:p.Thr98=
XR_429088.1:n.1278C=
XM_024448910.1:c.1115C=	XP_024304678.1:p.Thr372=
XM_024448911.1:c.602C=	XP_024304679.1:p.Thr201=
XM_024448912.1:c.293C=	XP_024304680.1:p.Thr98=
NM_012463.4:c.1115C= MANE Select	NP_036595.2:p.Thr372=