Canonical Allele Identifier: CA1232986977
Gene: ACP1 HGNC NCBI
SCARNA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.272938A= , CM000664.2:g.272938A= GRCh38
NC_000002.11:g.272938A= , CM000664.1:g.272938A= GRCh37
NC_000002.10:g.262938A= NCBI36
NG_012035.1:g.13070A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272067.11:c.231+633A= (ACP1) ENSP00000272067.6:n.231+633A=
ENST00000272065.10:c.231+788A= (ACP1) MANE Select ENSP00000272065.5:n.231+788A=
ENST00000272065.9:c.231+788A= (ACP1) ENSP00000272065.5:n.231+788A=
ENST00000272067.10:c.231+633A= (ACP1) ENSP00000272067.6:n.231+633A=
ENST00000405233.5:c.*680A= (ACP1) ENSP00000384307.1:n.*680A=
ENST00000405364.2:c.*166+633A= (ACP1) ENSP00000384184.2:n.*166+633A=
ENST00000413140.5:c.231+788A= (ACP1) ENSP00000410331.1:n.231+788A=
ENST00000442386.5:c.*137+788A= (ACP1) ENSP00000389681.1:n.*137+788A=
ENST00000453390.5:c.260+633A= (ACP1) ENSP00000411121.1:n.260+633A=
ENST00000480874.5:n.260+788A= (ACP1)
ENST00000484464.5:n.262+788A= (ACP1)
NM_004300.3:c.231+788A= (SCARNA10) NP_004291.1:n.231+788A=
NM_007099.3:c.231+633A= (SCARNA10) NP_009030.1:n.231+633A=
NR_024080.1:n.356+633A= (SCARNA10)
XM_011510363.1:c.231+633A= (SCARNA10) XP_011508665.1:n.231+633A=
XR_922680.1:n.987+633A= (SCARNA10)
XR_001738777.1:n.451+633A= (SCARNA10)
NM_004300.4:c.231+788A= (SCARNA10) MANE Select NP_004291.1:n.231+788A=
NM_007099.4:c.231+633A= (SCARNA10) NP_009030.1:n.231+633A=
NR_024080.2:n.278+633A= (SCARNA10)