Canonical Allele Identifier: CA711502293

Gene: ATP10A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.25730061C>G , CM000677.2:g.25730061C>G	GRCh38
NC_000015.9:g.25975208C>G , CM000677.1:g.25975208C>G	GRCh37
NC_000015.8:g.23526301C>G	NCBI36
NG_009282.1:g.138142G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555815.7:c.741-2795G>C MANE Select	ENSP00000450480.2:n.741-2795G>C
ENST00000356865.11:c.741-2795G>C	ENSP00000349325.6:n.741-2795G>C
ENST00000555815.6:c.741-2795G>C	ENSP00000450480.2:n.741-2795G>C
ENST00000620538.2:n.741-2795G>C
ENST00000673676.1:c.86-2795G>C
ENST00000673716.1:c.741-2795G>C	ENSP00000501027.1:n.741-2795G>C
ENST00000673747.1:c.741-2795G>C	ENSP00000501230.1:n.741-2795G>C
ENST00000673763.1:c.300-2795G>C	ENSP00000500973.1:n.300-2795G>C
ENST00000673898.1:n.1041-2795G>C
ENST00000356865.10:c.741-2795G>C	ENSP00000349325.6:n.741-2795G>C
ENST00000555815.5:c.741-2795G>C	ENSP00000450480.1:n.741-2795G>C
NM_024490.3:c.741-2795G>C	NP_077816.1:n.741-2795G>C
XM_005268261.3:c.741-2795G>C	XP_005268318.1:n.741-2795G>C
XM_006720619.2:c.741-2795G>C	XP_006720682.1:n.741-2795G>C
XM_011521826.1:c.741-2795G>C	XP_011520128.1:n.741-2795G>C
XM_011521827.1:c.741-2795G>C	XP_011520129.1:n.741-2795G>C
XM_011521828.1:c.741-2795G>C	XP_011520130.1:n.741-2795G>C
XM_011521829.1:c.-68-3979G>C	XP_011520131.1:n.-68-3979G>C
XM_005268261.4:c.741-2795G>C	XP_005268318.1:n.741-2795G>C
XM_011521826.2:c.741-2795G>C	XP_011520128.1:n.741-2795G>C
XM_011521828.2:c.741-2795G>C	XP_011520130.1:n.741-2795G>C
XM_011521829.2:c.-68-3979G>C	XP_011520131.1:n.-68-3979G>C
XM_017022436.1:c.300-2795G>C	XP_016877925.1:n.300-2795G>C
XM_017022437.1:c.-175-2795G>C	XP_016877926.1:n.-175-2795G>C
XR_001751366.1:n.1578-2795G>C
XR_001751367.1:n.1579-2795G>C
XR_001751368.1:n.1581-2795G>C
NM_024490.4:c.741-2795G>C MANE Select	NP_077816.1:n.741-2795G>C