Canonical Allele Identifier: CA1746790339
Gene: ATP6V0A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138762246C= , CM000669.2:g.138762246C= GRCh38
NC_000007.13:g.138446991C= , CM000669.1:g.138446991C= GRCh37
NC_000007.12:g.138097531C= NCBI36
NG_008145.1:g.40951G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310018.7:c.512+94G= MANE Select ENSP00000308122.2:n.512+94G=
ENST00000645515.1:c.512+94G= ENSP00000496421.1:n.512+94G=
ENST00000310018.6:c.512+94G= ENSP00000308122.2:n.512+94G=
ENST00000353492.4:c.512+94G= ENSP00000253856.6:n.512+94G=
ENST00000393054.5:c.512+94G= ENSP00000376774.1:n.512+94G=
ENST00000483139.1:n.761+94G=
NM_020632.2:c.512+94G= NP_065683.2:n.512+94G=
NM_130840.2:c.512+94G= NP_570855.2:n.512+94G=
NM_130841.2:c.512+94G= NP_570856.2:n.512+94G=
XM_005250393.1:c.512+94G= XP_005250450.1:n.512+94G=
XM_005250394.2:c.512+94G= XP_005250451.1:n.512+94G=
XM_005250394.3:c.512+94G= XP_005250451.1:n.512+94G=
NM_020632.3:c.512+94G= MANE Select NP_065683.2:n.512+94G=
NM_130840.3:c.512+94G= NP_570855.2:n.512+94G=
NM_130841.3:c.512+94G= NP_570856.2:n.512+94G=