Canonical Allele Identifier: CA369377666

Gene: ATP6V0A4

Linked Data

• MyVariant Identifiers: chr7:g.138447767C>T (hg19) ; chr7:g.138763022C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138763022C>T , CM000669.2:g.138763022C>T	GRCh38
NC_000007.13:g.138447767C>T , CM000669.1:g.138447767C>T	GRCh37
NC_000007.12:g.138098307C>T	NCBI36
NG_008145.1:g.40175G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.295G>A MANE Select	ENSP00000308122.2:p.Val99Ile
ENST00000645515.1:c.295G>A	ENSP00000496421.1:p.Val99Ile
ENST00000310018.6:c.295G>A	ENSP00000308122.2:p.Val99Ile
ENST00000353492.4:c.295G>A	ENSP00000253856.6:p.Val99Ile
ENST00000393054.5:c.295G>A	ENSP00000376774.1:p.Val99Ile
ENST00000483139.1:n.544G>A
NM_020632.2:c.295G>A	NP_065683.2:p.Val99Ile
NM_130840.2:c.295G>A	NP_570855.2:p.Val99Ile
NM_130841.2:c.295G>A	NP_570856.2:p.Val99Ile
XM_005250393.1:c.295G>A	XP_005250450.1:p.Val99Ile
XM_005250394.2:c.295G>A	XP_005250451.1:p.Val99Ile
XM_005250394.3:c.295G>A	XP_005250451.1:p.Val99Ile
NM_020632.3:c.295G>A MANE Select	NP_065683.2:p.Val99Ile
NM_130840.3:c.295G>A	NP_570855.2:p.Val99Ile
NM_130841.3:c.295G>A	NP_570856.2:p.Val99Ile