Canonical Allele Identifier: CA2748574341

Gene: ACP1 SCARNA10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.272926_272927insG , CM000664.2:g.272926_272927insG	GRCh38
NC_000002.11:g.272926_272927insG , CM000664.1:g.272926_272927insG	GRCh37
NC_000002.10:g.262926_262927insG	NCBI36
NG_012035.1:g.13058_13059insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272067.11:c.231+621_231+622insG (ACP1)	ENSP00000272067.6:n.231+621_231+622insG
ENST00000272065.10:c.231+776_231+777insG (ACP1) MANE Select	ENSP00000272065.5:n.231+776_231+777insG
ENST00000272065.9:c.231+776_231+777insG (ACP1)	ENSP00000272065.5:n.231+776_231+777insG
ENST00000272067.10:c.231+621_231+622insG (ACP1)	ENSP00000272067.6:n.231+621_231+622insG
ENST00000405233.5:c.*668_*669insG (ACP1)	ENSP00000384307.1:n.*668_*669insG
ENST00000405364.2:c.*166+621_*166+622insG (ACP1)	ENSP00000384184.2:n.*166+621_*166+622insG
ENST00000413140.5:c.231+776_231+777insG (ACP1)	ENSP00000410331.1:n.231+776_231+777insG
ENST00000442386.5:c.*137+776_*137+777insG (ACP1)	ENSP00000389681.1:n.*137+776_*137+777insG
ENST00000453390.5:c.260+621_260+622insG (ACP1)	ENSP00000411121.1:n.260+621_260+622insG
ENST00000480874.5:n.260+776_260+777insG (ACP1)
ENST00000484464.5:n.262+776_262+777insG (ACP1)
NM_004300.3:c.231+776_231+777insG (SCARNA10)	NP_004291.1:n.231+776_231+777insG
NM_007099.3:c.231+621_231+622insG (SCARNA10)	NP_009030.1:n.231+621_231+622insG
NR_024080.1:n.356+621_356+622insG (SCARNA10)
XM_011510363.1:c.231+621_231+622insG (SCARNA10)	XP_011508665.1:n.231+621_231+622insG
XR_922680.1:n.987+621_987+622insG (SCARNA10)
XR_001738777.1:n.451+621_451+622insG (SCARNA10)
NM_004300.4:c.231+776_231+777insG (SCARNA10) MANE Select	NP_004291.1:n.231+776_231+777insG
NM_007099.4:c.231+621_231+622insG (SCARNA10)	NP_009030.1:n.231+621_231+622insG
NR_024080.2:n.278+621_278+622insG (SCARNA10)