Canonical Allele Identifier: CA369379479

Gene: ATP6V0A4

Linked Data

• MyVariant Identifiers: chr7:g.138417825T>A (hg19) ; chr7:g.138733080T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138733080T>A , CM000669.2:g.138733080T>A	GRCh38
NC_000007.13:g.138417825T>A , CM000669.1:g.138417825T>A	GRCh37
NC_000007.12:g.138068365T>A	NCBI36
NG_008145.1:g.70117A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310018.7:c.1705A>T MANE Select	ENSP00000308122.2:p.Thr569Ser
ENST00000478480.2:c.931A>T	ENSP00000495261.1:p.Thr311Ser
ENST00000644341.1:c.931A>T	ENSP00000495642.1:p.Thr311Ser
ENST00000645515.1:c.1705A>T	ENSP00000496421.1:p.Thr569Ser
ENST00000647427.1:c.598A>T	ENSP00000496259.1:p.Thr200Ser
ENST00000310018.6:c.1705A>T	ENSP00000308122.2:p.Thr569Ser
ENST00000353492.4:c.1705A>T	ENSP00000253856.6:p.Thr569Ser
ENST00000393054.5:c.1705A>T	ENSP00000376774.1:p.Thr569Ser
NM_020632.2:c.1705A>T	NP_065683.2:p.Thr569Ser
NM_130840.2:c.1705A>T	NP_570855.2:p.Thr569Ser
NM_130841.2:c.1705A>T	NP_570856.2:p.Thr569Ser
XM_005250393.1:c.1705A>T	XP_005250450.1:p.Thr569Ser
XM_005250394.2:c.1705A>T	XP_005250451.1:p.Thr569Ser
XM_005250394.3:c.1705A>T	XP_005250451.1:p.Thr569Ser
NM_020632.3:c.1705A>T MANE Select	NP_065683.2:p.Thr569Ser
NM_130840.3:c.1705A>T	NP_570855.2:p.Thr569Ser
NM_130841.3:c.1705A>T	NP_570856.2:p.Thr569Ser