Canonical Allele Identifier: CA2657618693

Gene: ACP1 SCARNA10

Linked Data

• gnomAD v4: 2-272918-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.272918G>T , CM000664.2:g.272918G>T	GRCh38
NC_000002.11:g.272918G>T , CM000664.1:g.272918G>T	GRCh37
NC_000002.10:g.262918G>T	NCBI36
NG_012035.1:g.13050G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272067.11:c.231+613G>T (ACP1)	ENSP00000272067.6:n.231+613G>T
ENST00000272065.10:c.231+768G>T (ACP1) MANE Select	ENSP00000272065.5:n.231+768G>T
ENST00000272065.9:c.231+768G>T (ACP1)	ENSP00000272065.5:n.231+768G>T
ENST00000272067.10:c.231+613G>T (ACP1)	ENSP00000272067.6:n.231+613G>T
ENST00000405233.5:c.*660G>T (ACP1)	ENSP00000384307.1:n.*660G>T
ENST00000405364.2:c.*166+613G>T (ACP1)	ENSP00000384184.2:n.*166+613G>T
ENST00000413140.5:c.231+768G>T (ACP1)	ENSP00000410331.1:n.231+768G>T
ENST00000442386.5:c.*137+768G>T (ACP1)	ENSP00000389681.1:n.*137+768G>T
ENST00000453390.5:c.260+613G>T (ACP1)	ENSP00000411121.1:n.260+613G>T
ENST00000480874.5:n.260+768G>T (ACP1)
ENST00000484464.5:n.262+768G>T (ACP1)
NM_004300.3:c.231+768G>T (SCARNA10)	NP_004291.1:n.231+768G>T
NM_007099.3:c.231+613G>T (SCARNA10)	NP_009030.1:n.231+613G>T
NR_024080.1:n.356+613G>T (SCARNA10)
XM_011510363.1:c.231+613G>T (SCARNA10)	XP_011508665.1:n.231+613G>T
XR_922680.1:n.987+613G>T (SCARNA10)
XR_001738777.1:n.451+613G>T (SCARNA10)
NM_004300.4:c.231+768G>T (SCARNA10) MANE Select	NP_004291.1:n.231+768G>T
NM_007099.4:c.231+613G>T (SCARNA10)	NP_009030.1:n.231+613G>T
NR_024080.2:n.278+613G>T (SCARNA10)