Canonical Allele Identifier: CA489233200

Gene: ATP10A

Linked Data

• dbSNP Id: rs3816800
• MyVariant Identifiers: chr15:g.25925094C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.25679947C>T , CM000677.2:g.25679947C>T	GRCh38
NC_000015.9:g.25925094C>T , CM000677.1:g.25925094C>T	GRCh37
NC_000015.8:g.23476187C>T	NCBI36
NG_009282.1:g.188256G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000555815.7:c.3894G>A MANE Select	ENSP00000450480.2:p.Arg1298=
ENST00000356865.11:c.3894G>A	ENSP00000349325.6:p.Arg1298=
ENST00000555450.2:n.1686G>A
ENST00000555815.6:c.3894G>A	ENSP00000450480.2:p.Arg1298=
ENST00000673680.1:n.4556G>A
ENST00000673805.1:n.3239G>A
ENST00000674021.1:n.2221G>A
ENST00000356865.10:c.3894G>A	ENSP00000349325.6:p.Arg1298=
ENST00000555815.5:c.*2108G>A	ENSP00000450480.1:n.*2108G>A
NM_024490.3:c.3894G>A	NP_077816.1:p.Arg1298=
XM_005268261.3:c.3894G>A	XP_005268318.1:p.Arg1298=
XM_011521826.1:c.3894G>A	XP_011520128.1:p.Arg1298=
XM_011521827.1:c.3894G>A	XP_011520129.1:p.Arg1298=
XM_011521828.1:c.3894G>A	XP_011520130.1:p.Arg1298=
XM_011521829.1:c.2979G>A	XP_011520131.1:p.Arg993=
XM_011521830.1:c.2556G>A	XP_011520132.1:p.Arg852=
XM_005268261.4:c.3894G>A	XP_005268318.1:p.Arg1298=
XM_011521826.2:c.3894G>A	XP_011520128.1:p.Arg1298=
XM_011521828.2:c.3894G>A	XP_011520130.1:p.Arg1298=
XM_011521829.2:c.2979G>A	XP_011520131.1:p.Arg993=
XM_011521830.2:c.2718G>A	XP_011520132.2:p.Arg906=
XM_017022436.1:c.3453G>A	XP_016877925.1:p.Arg1151=
XM_017022437.1:c.2979G>A	XP_016877926.1:p.Arg993=
NM_024490.4:c.3894G>A MANE Select	NP_077816.1:p.Arg1298=