Canonical Allele Identifier: CA387155844

Gene: ATP6V0A2

Linked Data

• MyVariant Identifiers: chr12:g.124228453G>C (hg19) ; chr12:g.123743906G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123743906G>C , CM000674.2:g.123743906G>C	GRCh38
NC_000012.11:g.124228453G>C , CM000674.1:g.124228453G>C	GRCh37
NC_000012.10:g.122794406G>C	NCBI36
NG_012743.1:g.36589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1160G>C MANE Select	ENSP00000332247.2:p.Gly387Ala
ENST00000540368.6:n.1191G>C
ENST00000674794.1:c.1248G>C
ENST00000675260.1:n.435G>C
ENST00000675344.1:c.*181G>C	ENSP00000501953.1:n.*181G>C
ENST00000330342.7:c.1160G>C	ENSP00000332247.2:p.Gly387Ala
ENST00000504192.2:c.770G>C	ENSP00000443441.1:p.Gly257Ala
ENST00000536426.1:n.177G>C
ENST00000545059.5:n.3796G>C
NM_012463.3:c.1160G>C	NP_036595.2:p.Gly387Ala
XM_005253563.1:c.1160G>C	XP_005253620.1:p.Gly387Ala
XM_006719317.2:c.647G>C	XP_006719380.1:p.Gly216Ala
XM_006719318.2:c.338G>C	XP_006719381.1:p.Gly113Ala
XR_429088.1:n.1323G>C
XM_024448910.1:c.1160G>C	XP_024304678.1:p.Gly387Ala
XM_024448911.1:c.647G>C	XP_024304679.1:p.Gly216Ala
XM_024448912.1:c.338G>C	XP_024304680.1:p.Gly113Ala
NM_012463.4:c.1160G>C MANE Select	NP_036595.2:p.Gly387Ala