Canonical Allele Identifier: CA387151870

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124209299G>C (hg19) ; chr12:g.123724752G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724752G>C , CM000674.2:g.123724752G>C	GRCh38
NC_000012.11:g.124209299G>C , CM000674.1:g.124209299G>C	GRCh37
NC_000012.10:g.122775252G>C	NCBI36
NG_012743.1:g.17435G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.393G>C MANE Select	ENSP00000332247.2:p.Met131Ile
ENST00000540368.6:n.424G>C
ENST00000613625.5:c.393G>C	ENSP00000482236.1:p.Met131Ile
ENST00000675344.1:c.393G>C	ENSP00000501953.1:p.Met131Ile
ENST00000330342.7:c.393G>C	ENSP00000332247.2:p.Met131Ile
ENST00000504192.2:c.3G>C	ENSP00000443441.1:p.Met1Ile
ENST00000540368.5:n.603G>C
ENST00000613625.4:c.393G>C	ENSP00000482236.1:p.Met131Ile
NM_012463.3:c.393G>C	NP_036595.2:p.Met131Ile
XM_005253563.1:c.393G>C	XP_005253620.1:p.Met131Ile
XM_006719317.2:c.-32G>C	XP_006719380.1:n.-32G>C
XR_429088.1:n.556G>C
XM_024448910.1:c.393G>C	XP_024304678.1:p.Met131Ile
XM_024448911.1:c.-32G>C	XP_024304679.1:n.-32G>C
NM_012463.4:c.393G>C MANE Select	NP_036595.2:p.Met131Ile