Canonical Allele Identifier: CA2069005342

Gene: ATP6V0A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744647G= , CM000674.2:g.123744647G=	GRCh38
NC_000012.11:g.124229194G= , CM000674.1:g.124229194G=	GRCh37
NC_000012.10:g.122795147G=	NCBI36
NG_012743.1:g.37330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1377G= MANE Select	ENSP00000332247.2:p.Leu459=
ENST00000540368.6:n.1408G=
ENST00000674794.1:c.1465G=
ENST00000675260.1:n.652G=
ENST00000675344.1:c.*398G=	ENSP00000501953.1:n.*398G=
ENST00000330342.7:c.1377G=	ENSP00000332247.2:p.Leu459=
ENST00000536426.1:n.394G=
ENST00000545059.5:n.4013G=
NM_012463.3:c.1377G=	NP_036595.2:p.Leu459=
XM_005253563.1:c.1377G=	XP_005253620.1:p.Leu459=
XM_006719317.2:c.864G=	XP_006719380.1:p.Leu288=
XM_006719318.2:c.555G=	XP_006719381.1:p.Leu185=
XR_429088.1:n.1540G=
XM_024448910.1:c.1377G=	XP_024304678.1:p.Leu459=
XM_024448911.1:c.864G=	XP_024304679.1:p.Leu288=
XM_024448912.1:c.555G=	XP_024304680.1:p.Leu185=
NM_012463.4:c.1377G= MANE Select	NP_036595.2:p.Leu459=