Canonical Allele Identifier: CA387157464

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124229196T>A (hg19) ; chr12:g.123744649T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744649T>A , CM000674.2:g.123744649T>A	GRCh38
NC_000012.11:g.124229196T>A , CM000674.1:g.124229196T>A	GRCh37
NC_000012.10:g.122795149T>A	NCBI36
NG_012743.1:g.37332T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1379T>A MANE Select	ENSP00000332247.2:p.Phe460Tyr
ENST00000540368.6:n.1410T>A
ENST00000674794.1:c.1467T>A
ENST00000675260.1:n.654T>A
ENST00000675344.1:c.*400T>A	ENSP00000501953.1:n.*400T>A
ENST00000330342.7:c.1379T>A	ENSP00000332247.2:p.Phe460Tyr
ENST00000536426.1:n.396T>A
ENST00000545059.5:n.4015T>A
NM_012463.3:c.1379T>A	NP_036595.2:p.Phe460Tyr
XM_005253563.1:c.1379T>A	XP_005253620.1:p.Phe460Tyr
XM_006719317.2:c.866T>A	XP_006719380.1:p.Phe289Tyr
XM_006719318.2:c.557T>A	XP_006719381.1:p.Phe186Tyr
XR_429088.1:n.1542T>A
XM_024448910.1:c.1379T>A	XP_024304678.1:p.Phe460Tyr
XM_024448911.1:c.866T>A	XP_024304679.1:p.Phe289Tyr
XM_024448912.1:c.557T>A	XP_024304680.1:p.Phe186Tyr
NM_012463.4:c.1379T>A MANE Select	NP_036595.2:p.Phe460Tyr