Canonical Allele Identifier: CA834045359

Gene: ATP6V0A4

Linked Data

• dbSNP Id: rs1396063802
• gnomAD v3: 7-138771073-A-C
• gnomAD v4: 7-138771073-A-C
• MyVariant Identifiers: chr7:g.138455818A>C (hg19) ; chr7:g.138771073A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138771073A>C , CM000669.2:g.138771073A>C	GRCh38
NC_000007.13:g.138455818A>C , CM000669.1:g.138455818A>C	GRCh37
NC_000007.12:g.138106358A>C	NCBI36
NG_008145.1:g.32124T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310018.7:c.117+58T>G MANE Select	ENSP00000308122.2:n.117+58T>G
ENST00000645515.1:c.117+58T>G	ENSP00000496421.1:n.117+58T>G
ENST00000310018.6:c.117+58T>G	ENSP00000308122.2:n.117+58T>G
ENST00000353492.4:c.117+58T>G	ENSP00000253856.6:n.117+58T>G
ENST00000393054.5:c.117+58T>G	ENSP00000376774.1:n.117+58T>G
ENST00000483139.1:n.366+58T>G
NM_020632.2:c.117+58T>G	NP_065683.2:n.117+58T>G
NM_130840.2:c.117+58T>G	NP_570855.2:n.117+58T>G
NM_130841.2:c.117+58T>G	NP_570856.2:n.117+58T>G
XM_005250393.1:c.117+58T>G	XP_005250450.1:n.117+58T>G
XM_005250394.2:c.117+58T>G	XP_005250451.1:n.117+58T>G
XM_005250394.3:c.117+58T>G	XP_005250451.1:n.117+58T>G
NM_020632.3:c.117+58T>G MANE Select	NP_065683.2:n.117+58T>G
NM_130840.3:c.117+58T>G	NP_570855.2:n.117+58T>G
NM_130841.3:c.117+58T>G	NP_570856.2:n.117+58T>G