Canonical Allele Identifier: CA2069004303
Gene: ATP6V0A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123744146C= , CM000674.2:g.123744146C= GRCh38
NC_000012.11:g.124228693C= , CM000674.1:g.124228693C= GRCh37
NC_000012.10:g.122794646C= NCBI36
NG_012743.1:g.36829C=

Transcript Alleles

HGVS Amino-acid change
ENST00000330342.8:c.1190-55C= MANE Select ENSP00000332247.2:n.1190-55C=
ENST00000540368.6:n.1221-55C=
ENST00000674794.1:c.1278-55C=
ENST00000675260.1:n.465-55C=
ENST00000675344.1:c.*211-55C= ENSP00000501953.1:n.*211-55C=
ENST00000330342.7:c.1190-55C= ENSP00000332247.2:n.1190-55C=
ENST00000504192.2:c.800-55C= ENSP00000443441.1:n.800-55C=
ENST00000536426.1:n.207-55C=
ENST00000545059.5:n.3826-55C=
NM_012463.3:c.1190-55C= NP_036595.2:n.1190-55C=
XM_005253563.1:c.1190-55C= XP_005253620.1:n.1190-55C=
XM_006719317.2:c.677-55C= XP_006719380.1:n.677-55C=
XM_006719318.2:c.368-55C= XP_006719381.1:n.368-55C=
XR_429088.1:n.1353-55C=
XM_024448910.1:c.1190-55C= XP_024304678.1:n.1190-55C=
XM_024448911.1:c.677-55C= XP_024304679.1:n.677-55C=
XM_024448912.1:c.368-55C= XP_024304680.1:n.368-55C=
NM_012463.4:c.1190-55C= MANE Select NP_036595.2:n.1190-55C=