Canonical Allele Identifier: CA387157453

Gene: ATP6V0A2

Linked Data

• dbSNP Id: rs1425437024
• gnomAD v2: 12-124229193-T-C
• gnomAD v4: 12-123744646-T-C
• MyVariant Identifiers: chr12:g.124229193T>C (hg19) ; chr12:g.123744646T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744646T>C , CM000674.2:g.123744646T>C	GRCh38
NC_000012.11:g.124229193T>C , CM000674.1:g.124229193T>C	GRCh37
NC_000012.10:g.122795146T>C	NCBI36
NG_012743.1:g.37329T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1376T>C MANE Select	ENSP00000332247.2:p.Leu459Pro
ENST00000540368.6:n.1407T>C
ENST00000674794.1:c.1464T>C
ENST00000675260.1:n.651T>C
ENST00000675344.1:c.*397T>C	ENSP00000501953.1:n.*397T>C
ENST00000330342.7:c.1376T>C	ENSP00000332247.2:p.Leu459Pro
ENST00000536426.1:n.393T>C
ENST00000545059.5:n.4012T>C
NM_012463.3:c.1376T>C	NP_036595.2:p.Leu459Pro
XM_005253563.1:c.1376T>C	XP_005253620.1:p.Leu459Pro
XM_006719317.2:c.863T>C	XP_006719380.1:p.Leu288Pro
XM_006719318.2:c.554T>C	XP_006719381.1:p.Leu185Pro
XR_429088.1:n.1539T>C
XM_024448910.1:c.1376T>C	XP_024304678.1:p.Leu459Pro
XM_024448911.1:c.863T>C	XP_024304679.1:p.Leu288Pro
XM_024448912.1:c.554T>C	XP_024304680.1:p.Leu185Pro
NM_012463.4:c.1376T>C MANE Select	NP_036595.2:p.Leu459Pro