Canonical Allele Identifier: CA2069004349
Gene: ATP6V0A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123744169G= , CM000674.2:g.123744169G= GRCh38
NC_000012.11:g.124228716G= , CM000674.1:g.124228716G= GRCh37
NC_000012.10:g.122794669G= NCBI36
NG_012743.1:g.36852G=

Transcript Alleles

HGVS Amino-acid change
ENST00000330342.8:c.1190-32G= MANE Select ENSP00000332247.2:n.1190-32G=
ENST00000540368.6:n.1221-32G=
ENST00000674794.1:c.1278-32G=
ENST00000675260.1:n.465-32G=
ENST00000675344.1:c.*211-32G= ENSP00000501953.1:n.*211-32G=
ENST00000330342.7:c.1190-32G= ENSP00000332247.2:n.1190-32G=
ENST00000504192.2:c.800-32G= ENSP00000443441.1:n.800-32G=
ENST00000536426.1:n.207-32G=
ENST00000545059.5:n.3826-32G=
NM_012463.3:c.1190-32G= NP_036595.2:n.1190-32G=
XM_005253563.1:c.1190-32G= XP_005253620.1:n.1190-32G=
XM_006719317.2:c.677-32G= XP_006719380.1:n.677-32G=
XM_006719318.2:c.368-32G= XP_006719381.1:n.368-32G=
XR_429088.1:n.1353-32G=
XM_024448910.1:c.1190-32G= XP_024304678.1:n.1190-32G=
XM_024448911.1:c.677-32G= XP_024304679.1:n.677-32G=
XM_024448912.1:c.368-32G= XP_024304680.1:n.368-32G=
NM_012463.4:c.1190-32G= MANE Select NP_036595.2:n.1190-32G=