Canonical Allele Identifier: CA482270238

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124209302G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724755G>T , CM000674.2:g.123724755G>T	GRCh38
NC_000012.11:g.124209302G>T , CM000674.1:g.124209302G>T	GRCh37
NC_000012.10:g.122775255G>T	NCBI36
NG_012743.1:g.17438G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.396G>T MANE Select	ENSP00000332247.2:p.Leu132=
ENST00000540368.6:n.427G>T
ENST00000613625.5:c.396G>T	ENSP00000482236.1:p.Leu132=
ENST00000675344.1:c.396G>T	ENSP00000501953.1:p.Leu132=
ENST00000330342.7:c.396G>T	ENSP00000332247.2:p.Leu132=
ENST00000504192.2:c.6G>T	ENSP00000443441.1:p.Leu2=
ENST00000540368.5:n.606G>T
ENST00000613625.4:c.396G>T	ENSP00000482236.1:p.Leu132=
NM_012463.3:c.396G>T	NP_036595.2:p.Leu132=
XM_005253563.1:c.396G>T	XP_005253620.1:p.Leu132=
XM_006719317.2:c.-29G>T	XP_006719380.1:n.-29G>T
XR_429088.1:n.559G>T
XM_024448910.1:c.396G>T	XP_024304678.1:p.Leu132=
XM_024448911.1:c.-29G>T	XP_024304679.1:n.-29G>T
NM_012463.4:c.396G>T MANE Select	NP_036595.2:p.Leu132=