Canonical Allele Identifier: CA1259810664

Gene: ATP6V1B1 VAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70958133G= , CM000664.2:g.70958133G=	GRCh38
NC_000002.11:g.71185263G= , CM000664.1:g.71185263G=	GRCh37
NC_000002.10:g.71038771G=	NCBI36
NG_008016.1:g.27266G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234396.10:c.262G= (ATP6V1B1) MANE Select	ENSP00000234396.4:p.Ala88=
ENST00000432098.2:n.428G= (ATP6V1B1)
ENST00000432367.6:c.466G= (VAX2)
ENST00000454446.6:c.262G= (ATP6V1B1)	ENSP00000408361.2:p.Ala88=
ENST00000646783.1:c.298G= (VAX2)
ENST00000234396.8:c.262G= (ATP6V1B1)	ENSP00000234396.4:p.Ala88=
ENST00000412314.5:c.262G= (ATP6V1B1)	ENSP00000388353.1:p.Ala88=
ENST00000432098.1:c.-99G= (ATP6V1B1)	ENSP00000387599.1:n.-99G=
ENST00000432367.5:c.262G= (ATP6V1B1)	ENSP00000405114.1:p.Ala88=
ENST00000453130.1:c.143-9758C=
ENST00000454446.5:c.313G= (ATP6V1B1)	ENSP00000408361.1:p.Ala105=
ENST00000463380.1:n.363G= (ATP6V1B1)
ENST00000606025.5:c.476-15700C=	ENSP00000475641.1:n.476-15700C=
NM_001692.3:c.262G= (ATP6V1B1)	NP_001683.2:p.Ala88=
XM_011532907.1:c.382G= (ATP6V1B1)	XP_011531209.1:p.Ala128=
NM_001692.4:c.262G= (ATP6V1B1) MANE Select	NP_001683.2:p.Ala88=
XM_011532907.2:c.382G= (ATP6V1B1)	XP_011531209.1:p.Ala128=