Canonical Allele Identifier: CA387157259

Gene: ATP6V0A2

Linked Data

• gnomAD v4: 12-123744605-G-T
• MyVariant Identifiers: chr12:g.124229152G>T (hg19) ; chr12:g.123744605G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744605G>T , CM000674.2:g.123744605G>T	GRCh38
NC_000012.11:g.124229152G>T , CM000674.1:g.124229152G>T	GRCh37
NC_000012.10:g.122795105G>T	NCBI36
NG_012743.1:g.37288G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1335G>T MANE Select	ENSP00000332247.2:p.Arg445Ser
ENST00000540368.6:n.1366G>T
ENST00000674794.1:c.1423G>T
ENST00000675260.1:n.610G>T
ENST00000675344.1:c.*356G>T	ENSP00000501953.1:n.*356G>T
ENST00000330342.7:c.1335G>T	ENSP00000332247.2:p.Arg445Ser
ENST00000504192.2:c.945G>T	ENSP00000443441.1:p.Arg315Ser
ENST00000536426.1:n.352G>T
ENST00000545059.5:n.3971G>T
NM_012463.3:c.1335G>T	NP_036595.2:p.Arg445Ser
XM_005253563.1:c.1335G>T	XP_005253620.1:p.Arg445Ser
XM_006719317.2:c.822G>T	XP_006719380.1:p.Arg274Ser
XM_006719318.2:c.513G>T	XP_006719381.1:p.Arg171Ser
XR_429088.1:n.1498G>T
XM_024448910.1:c.1335G>T	XP_024304678.1:p.Arg445Ser
XM_024448911.1:c.822G>T	XP_024304679.1:p.Arg274Ser
XM_024448912.1:c.513G>T	XP_024304680.1:p.Arg171Ser
NM_012463.4:c.1335G>T MANE Select	NP_036595.2:p.Arg445Ser