Canonical Allele Identifier: CA2685129794
Gene: ATP6V0A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138762450_138762472del , CM000669.2:g.138762450_138762472del GRCh38
NC_000007.13:g.138447195_138447217del , CM000669.1:g.138447195_138447217del GRCh37
NC_000007.12:g.138097735_138097757del NCBI36
NG_008145.1:g.40725_40747del

Transcript Alleles

HGVS Amino-acid change
ENST00000310018.7:c.418-38_418-16del MANE Select ENSP00000308122.2:n.418-38_418-16del
ENST00000645515.1:c.418-38_418-16del ENSP00000496421.1:n.418-38_418-16del
ENST00000310018.6:c.418-38_418-16del ENSP00000308122.2:n.418-38_418-16del
ENST00000353492.4:c.418-38_418-16del ENSP00000253856.6:n.418-38_418-16del
ENST00000393054.5:c.418-38_418-16del ENSP00000376774.1:n.418-38_418-16del
ENST00000483139.1:n.667-38_667-16del
NM_020632.2:c.418-38_418-16del NP_065683.2:n.418-38_418-16del
NM_130840.2:c.418-38_418-16del NP_570855.2:n.418-38_418-16del
NM_130841.2:c.418-38_418-16del NP_570856.2:n.418-38_418-16del
XM_005250393.1:c.418-38_418-16del XP_005250450.1:n.418-38_418-16del
XM_005250394.2:c.418-38_418-16del XP_005250451.1:n.418-38_418-16del
XM_005250394.3:c.418-38_418-16del XP_005250451.1:n.418-38_418-16del
NM_020632.3:c.418-38_418-16del MANE Select NP_065683.2:n.418-38_418-16del
NM_130840.3:c.418-38_418-16del NP_570855.2:n.418-38_418-16del
NM_130841.3:c.418-38_418-16del NP_570856.2:n.418-38_418-16del