Canonical Allele Identifier: CA2685127632
Gene: ATP6V0A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138732806_138732807insAT , CM000669.2:g.138732806_138732807insAT GRCh38
NC_000007.13:g.138417551_138417552insAT , CM000669.1:g.138417551_138417552insAT GRCh37
NC_000007.12:g.138068091_138068092insAT NCBI36
NG_008145.1:g.70390_70391insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000310018.7:c.1908+70_1908+71insAT MANE Select ENSP00000308122.2:n.1908+70_1908+71insAT
ENST00000478480.2:c.1134+70_1134+71insAT ENSP00000495261.1:n.1134+70_1134+71insAT
ENST00000644341.1:c.1134+70_1134+71insAT ENSP00000495642.1:n.1134+70_1134+71insAT
ENST00000645515.1:c.1908+70_1908+71insAT ENSP00000496421.1:n.1908+70_1908+71insAT
ENST00000647427.1:c.801+70_801+71insAT ENSP00000496259.1:n.801+70_801+71insAT
ENST00000310018.6:c.1908+70_1908+71insAT ENSP00000308122.2:n.1908+70_1908+71insAT
ENST00000353492.4:c.1908+70_1908+71insAT ENSP00000253856.6:n.1908+70_1908+71insAT
ENST00000393054.5:c.1908+70_1908+71insAT ENSP00000376774.1:n.1908+70_1908+71insAT
NM_020632.2:c.1908+70_1908+71insAT NP_065683.2:n.1908+70_1908+71insAT
NM_130840.2:c.1908+70_1908+71insAT NP_570855.2:n.1908+70_1908+71insAT
NM_130841.2:c.1908+70_1908+71insAT NP_570856.2:n.1908+70_1908+71insAT
XM_005250393.1:c.1908+70_1908+71insAT XP_005250450.1:n.1908+70_1908+71insAT
XM_005250394.2:c.1908+70_1908+71insAT XP_005250451.1:n.1908+70_1908+71insAT
XM_005250394.3:c.1908+70_1908+71insAT XP_005250451.1:n.1908+70_1908+71insAT
NM_020632.3:c.1908+70_1908+71insAT MANE Select NP_065683.2:n.1908+70_1908+71insAT
NM_130840.3:c.1908+70_1908+71insAT NP_570855.2:n.1908+70_1908+71insAT
NM_130841.3:c.1908+70_1908+71insAT NP_570856.2:n.1908+70_1908+71insAT