Canonical Allele Identifier: CA482452192

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124229146C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744599C>T , CM000674.2:g.123744599C>T	GRCh38
NC_000012.11:g.124229146C>T , CM000674.1:g.124229146C>T	GRCh37
NC_000012.10:g.122795099C>T	NCBI36
NG_012743.1:g.37282C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1329C>T MANE Select	ENSP00000332247.2:p.Ile443=
ENST00000540368.6:n.1360C>T
ENST00000674794.1:c.1417C>T
ENST00000675260.1:n.604C>T
ENST00000675344.1:c.*350C>T	ENSP00000501953.1:n.*350C>T
ENST00000330342.7:c.1329C>T	ENSP00000332247.2:p.Ile443=
ENST00000504192.2:c.939C>T	ENSP00000443441.1:p.Ile313=
ENST00000536426.1:n.346C>T
ENST00000545059.5:n.3965C>T
NM_012463.3:c.1329C>T	NP_036595.2:p.Ile443=
XM_005253563.1:c.1329C>T	XP_005253620.1:p.Ile443=
XM_006719317.2:c.816C>T	XP_006719380.1:p.Ile272=
XM_006719318.2:c.507C>T	XP_006719381.1:p.Ile169=
XR_429088.1:n.1492C>T
XM_024448910.1:c.1329C>T	XP_024304678.1:p.Ile443=
XM_024448911.1:c.816C>T	XP_024304679.1:p.Ile272=
XM_024448912.1:c.507C>T	XP_024304680.1:p.Ile169=
NM_012463.4:c.1329C>T MANE Select	NP_036595.2:p.Ile443=