Canonical Allele Identifier: CA482270249

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124209320T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123724773T>C , CM000674.2:g.123724773T>C	GRCh38
NC_000012.11:g.124209320T>C , CM000674.1:g.124209320T>C	GRCh37
NC_000012.10:g.122775273T>C	NCBI36
NG_012743.1:g.17456T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.414T>C MANE Select	ENSP00000332247.2:p.Phe138=
ENST00000540368.6:n.445T>C
ENST00000613625.5:c.414T>C	ENSP00000482236.1:p.Phe138=
ENST00000675344.1:c.414T>C	ENSP00000501953.1:p.Phe138=
ENST00000330342.7:c.414T>C	ENSP00000332247.2:p.Phe138=
ENST00000504192.2:c.24T>C	ENSP00000443441.1:p.Phe8=
ENST00000540368.5:n.624T>C
ENST00000613625.4:c.414T>C	ENSP00000482236.1:p.Phe138=
NM_012463.3:c.414T>C	NP_036595.2:p.Phe138=
XM_005253563.1:c.414T>C	XP_005253620.1:p.Phe138=
XM_006719317.2:c.-11T>C	XP_006719380.1:n.-11T>C
XR_429088.1:n.577T>C
XM_024448910.1:c.414T>C	XP_024304678.1:p.Phe138=
XM_024448911.1:c.-11T>C	XP_024304679.1:n.-11T>C
NM_012463.4:c.414T>C MANE Select	NP_036595.2:p.Phe138=