Canonical Allele Identifier: CA387157524

Gene: ATP6V0A2

Linked Data

• dbSNP Id: rs1956642501
• gnomAD v4: 12-123744660-A-G
• COSMIC: COSM1677458
• MyVariant Identifiers: chr12:g.124229207A>G (hg19) ; chr12:g.123744660A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744660A>G , CM000674.2:g.123744660A>G	GRCh38
NC_000012.11:g.124229207A>G , CM000674.1:g.124229207A>G	GRCh37
NC_000012.10:g.122795160A>G	NCBI36
NG_012743.1:g.37343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1390A>G MANE Select	ENSP00000332247.2:p.Thr464Ala
ENST00000540368.6:n.1421A>G
ENST00000674794.1:c.1478A>G
ENST00000675260.1:n.665A>G
ENST00000675344.1:c.*411A>G	ENSP00000501953.1:n.*411A>G
ENST00000330342.7:c.1390A>G	ENSP00000332247.2:p.Thr464Ala
ENST00000536426.1:n.407A>G
ENST00000545059.5:n.4026A>G
NM_012463.3:c.1390A>G	NP_036595.2:p.Thr464Ala
XM_005253563.1:c.1390A>G	XP_005253620.1:p.Thr464Ala
XM_006719317.2:c.877A>G	XP_006719380.1:p.Thr293Ala
XM_006719318.2:c.568A>G	XP_006719381.1:p.Thr190Ala
XR_429088.1:n.1553A>G
XM_024448910.1:c.1390A>G	XP_024304678.1:p.Thr464Ala
XM_024448911.1:c.877A>G	XP_024304679.1:p.Thr293Ala
XM_024448912.1:c.568A>G	XP_024304680.1:p.Thr190Ala
NM_012463.4:c.1390A>G MANE Select	NP_036595.2:p.Thr464Ala