Canonical Allele Identifier: CA387153801

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124220078C>G (hg19) ; chr12:g.123735531C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123735531C>G , CM000674.2:g.123735531C>G	GRCh38
NC_000012.11:g.124220078C>G , CM000674.1:g.124220078C>G	GRCh37
NC_000012.10:g.122786031C>G	NCBI36
NG_012743.1:g.28214C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.732C>G MANE Select	ENSP00000332247.2:p.Cys244Trp
ENST00000540368.6:n.763C>G
ENST00000613625.5:c.732C>G	ENSP00000482236.1:p.Cys244Trp
ENST00000674794.1:c.172C>G
ENST00000675344.1:c.732C>G	ENSP00000501953.1:p.Cys244Trp
ENST00000330342.7:c.732C>G	ENSP00000332247.2:p.Cys244Trp
ENST00000504192.2:c.342C>G	ENSP00000443441.1:p.Cys114Trp
ENST00000540368.5:n.942C>G
ENST00000545059.5:n.3368C>G
ENST00000613625.4:c.732C>G	ENSP00000482236.1:p.Cys244Trp
NM_012463.3:c.732C>G	NP_036595.2:p.Cys244Trp
XM_005253563.1:c.732C>G	XP_005253620.1:p.Cys244Trp
XM_006719317.2:c.219C>G	XP_006719380.1:p.Cys73Trp
XR_429088.1:n.895C>G
XM_024448910.1:c.732C>G	XP_024304678.1:p.Cys244Trp
XM_024448911.1:c.219C>G	XP_024304679.1:p.Cys73Trp
NM_012463.4:c.732C>G MANE Select	NP_036595.2:p.Cys244Trp