Canonical Allele Identifier: CA387156542

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124228807C>G (hg19) ; chr12:g.123744260C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744260C>G , CM000674.2:g.123744260C>G	GRCh38
NC_000012.11:g.124228807C>G , CM000674.1:g.124228807C>G	GRCh37
NC_000012.10:g.122794760C>G	NCBI36
NG_012743.1:g.36943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1249C>G MANE Select	ENSP00000332247.2:p.His417Asp
ENST00000540368.6:n.1280C>G
ENST00000674794.1:c.1337C>G
ENST00000675260.1:n.524C>G
ENST00000675344.1:c.*270C>G	ENSP00000501953.1:n.*270C>G
ENST00000330342.7:c.1249C>G	ENSP00000332247.2:p.His417Asp
ENST00000504192.2:c.859C>G	ENSP00000443441.1:p.His287Asp
ENST00000536426.1:n.266C>G
ENST00000545059.5:n.3885C>G
NM_012463.3:c.1249C>G	NP_036595.2:p.His417Asp
XM_005253563.1:c.1249C>G	XP_005253620.1:p.His417Asp
XM_006719317.2:c.736C>G	XP_006719380.1:p.His246Asp
XM_006719318.2:c.427C>G	XP_006719381.1:p.His143Asp
XR_429088.1:n.1412C>G
XM_024448910.1:c.1249C>G	XP_024304678.1:p.His417Asp
XM_024448911.1:c.736C>G	XP_024304679.1:p.His246Asp
XM_024448912.1:c.427C>G	XP_024304680.1:p.His143Asp
NM_012463.4:c.1249C>G MANE Select	NP_036595.2:p.His417Asp