Canonical Allele Identifier: CA387156535

Gene: ATP6V0A2

Linked Data

• gnomAD v4: 12-123744258-G-T
• MyVariant Identifiers: chr12:g.124228805G>T (hg19) ; chr12:g.123744258G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744258G>T , CM000674.2:g.123744258G>T	GRCh38
NC_000012.11:g.124228805G>T , CM000674.1:g.124228805G>T	GRCh37
NC_000012.10:g.122794758G>T	NCBI36
NG_012743.1:g.36941G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1247G>T MANE Select	ENSP00000332247.2:p.Gly416Val
ENST00000540368.6:n.1278G>T
ENST00000674794.1:c.1335G>T
ENST00000675260.1:n.522G>T
ENST00000675344.1:c.*268G>T	ENSP00000501953.1:n.*268G>T
ENST00000330342.7:c.1247G>T	ENSP00000332247.2:p.Gly416Val
ENST00000504192.2:c.857G>T	ENSP00000443441.1:p.Gly286Val
ENST00000536426.1:n.264G>T
ENST00000545059.5:n.3883G>T
NM_012463.3:c.1247G>T	NP_036595.2:p.Gly416Val
XM_005253563.1:c.1247G>T	XP_005253620.1:p.Gly416Val
XM_006719317.2:c.734G>T	XP_006719380.1:p.Gly245Val
XM_006719318.2:c.425G>T	XP_006719381.1:p.Gly142Val
XR_429088.1:n.1410G>T
XM_024448910.1:c.1247G>T	XP_024304678.1:p.Gly416Val
XM_024448911.1:c.734G>T	XP_024304679.1:p.Gly245Val
XM_024448912.1:c.425G>T	XP_024304680.1:p.Gly142Val
NM_012463.4:c.1247G>T MANE Select	NP_036595.2:p.Gly416Val