Canonical Allele Identifier: CA578206061

Gene: ATP6V0A4

Linked Data

• dbSNP Id: rs762191582
• gnomAD v2: 7-138447636-C-A
• gnomAD v3: 7-138762891-C-A
• gnomAD v4: 7-138762891-C-A
• MyVariant Identifiers: chr7:g.138447636C>A (hg19) ; chr7:g.138762891C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138762891C>A , CM000669.2:g.138762891C>A	GRCh38
NC_000007.13:g.138447636C>A , CM000669.1:g.138447636C>A	GRCh37
NC_000007.12:g.138098176C>A	NCBI36
NG_008145.1:g.40306G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310018.7:c.417+9G>T MANE Select	ENSP00000308122.2:n.417+9G>T
ENST00000645515.1:c.417+9G>T	ENSP00000496421.1:n.417+9G>T
ENST00000310018.6:c.417+9G>T	ENSP00000308122.2:n.417+9G>T
ENST00000353492.4:c.417+9G>T	ENSP00000253856.6:n.417+9G>T
ENST00000393054.5:c.417+9G>T	ENSP00000376774.1:n.417+9G>T
ENST00000483139.1:n.666+9G>T
NM_020632.2:c.417+9G>T	NP_065683.2:n.417+9G>T
NM_130840.2:c.417+9G>T	NP_570855.2:n.417+9G>T
NM_130841.2:c.417+9G>T	NP_570856.2:n.417+9G>T
XM_005250393.1:c.417+9G>T	XP_005250450.1:n.417+9G>T
XM_005250394.2:c.417+9G>T	XP_005250451.1:n.417+9G>T
XM_005250394.3:c.417+9G>T	XP_005250451.1:n.417+9G>T
NM_020632.3:c.417+9G>T MANE Select	NP_065683.2:n.417+9G>T
NM_130840.3:c.417+9G>T	NP_570855.2:n.417+9G>T
NM_130841.3:c.417+9G>T	NP_570856.2:n.417+9G>T