Canonical Allele Identifier: CA2621700688

Gene: ATP6V0A2

Linked Data

• gnomAD v4: 12-123743768-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743768C>A , CM000674.2:g.123743768C>A	GRCh38
NC_000012.11:g.124228315C>A , CM000674.1:g.124228315C>A	GRCh37
NC_000012.10:g.122794268C>A	NCBI36
NG_012743.1:g.36451C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330342.8:c.1039-17C>A MANE Select	ENSP00000332247.2:n.1039-17C>A
ENST00000540368.6:n.1070-17C>A
ENST00000674794.1:c.1127-17C>A
ENST00000675260.1:n.297C>A
ENST00000675344.1:c.*60-17C>A	ENSP00000501953.1:n.*60-17C>A
ENST00000330342.7:c.1039-17C>A	ENSP00000332247.2:n.1039-17C>A
ENST00000504192.2:c.649-17C>A	ENSP00000443441.1:n.649-17C>A
ENST00000536426.1:n.56-17C>A
ENST00000545059.5:n.3675-17C>A
NM_012463.3:c.1039-17C>A	NP_036595.2:n.1039-17C>A
XM_005253563.1:c.1039-17C>A	XP_005253620.1:n.1039-17C>A
XM_006719317.2:c.526-17C>A	XP_006719380.1:n.526-17C>A
XM_006719318.2:c.217-17C>A	XP_006719381.1:n.217-17C>A
XR_429088.1:n.1202-17C>A
XM_024448910.1:c.1039-17C>A	XP_024304678.1:n.1039-17C>A
XM_024448911.1:c.526-17C>A	XP_024304679.1:n.526-17C>A
XM_024448912.1:c.217-17C>A	XP_024304680.1:n.217-17C>A
NM_012463.4:c.1039-17C>A MANE Select	NP_036595.2:n.1039-17C>A