Canonical Allele Identifier: CA2659051971

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254473-C-CGGTGGCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254473_54254474insGGTGGCCG , CM000664.2:g.54254473_54254474insGGTGGCCG	GRCh38
NC_000002.11:g.54481610_54481611insGGTGGCCG , CM000664.1:g.54481610_54481611insGGTGGCCG	GRCh37
NC_000002.10:g.54335114_54335115insGGTGGCCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50215_186-50214insGGTGGCCG (ACYP2) MANE Select	ENSP00000378161.3:n.186-50215_186-50214insGGTGGCCG
ENST00000394666.8:c.186-50215_186-50214insGGTGGCCG (ACYP2)	ENSP00000378161.3:n.186-50215_186-50214insGGTGGCCG
ENST00000317802.9:c.*445_*446insCGGCCACC (TSPYL6) MANE Select	ENSP00000417919.2:n.*445_*446insCGGCCACC
ENST00000607452.6:c.405-50215_405-50214insGGTGGCCG (ACYP2)	ENSP00000475986.1:n.405-50215_405-50214insGGTGGCCG
ENST00000303536.8:c.270-12823_270-12822insGGTGGCCG (ACYP2)	ENSP00000306448.4:n.270-12823_270-12822insGGTGGCCG
ENST00000317802.8:c.*445_*446insCGGCCACC (TSPYL6)	ENSP00000417919.2:n.*445_*446insCGGCCACC
ENST00000394666.7:c.186-50215_186-50214insGGTGGCCG (ACYP2)	ENSP00000378161.3:n.186-50215_186-50214insGGTGGCCG
ENST00000494922.6:c.265+31390_265+31391insGGTGGCCG (ACYP2)
ENST00000606865.1:c.138-50215_138-50214insGGTGGCCG (ACYP2)	ENSP00000475333.1:n.138-50215_138-50214insGGTGGCCG
ENST00000607452.5:c.405-50215_405-50214insGGTGGCCG (ACYP2)	ENSP00000475986.1:n.405-50215_405-50214insGGTGGCCG
NM_001003937.2:c.*445_*446insCGGCCACC (TSPYL6)	NP_001003937.2:n.*445_*446insCGGCCACC
NM_138448.3:c.186-50215_186-50214insGGTGGCCG (ACYP2)	NP_612457.1:n.186-50215_186-50214insGGTGGCCG
NM_001320586.1:c.405-50215_405-50214insGGTGGCCG (ACYP2)	NP_001307515.1:n.405-50215_405-50214insGGTGGCCG
NM_001320587.1:c.312-50215_312-50214insGGTGGCCG (ACYP2)	NP_001307516.1:n.312-50215_312-50214insGGTGGCCG
NM_001320588.1:c.114-50215_114-50214insGGTGGCCG (ACYP2)	NP_001307517.1:n.114-50215_114-50214insGGTGGCCG
NM_001320589.1:c.186-12823_186-12822insGGTGGCCG (ACYP2)	NP_001307518.1:n.186-12823_186-12822insGGTGGCCG
XM_017005411.1:c.486-50215_486-50214insGGTGGCCG (ACYP2)	XP_016860900.1:n.486-50215_486-50214insGGTGGCCG
XM_017005412.1:c.486-12823_486-12822insGGTGGCCG (ACYP2)	XP_016860901.1:n.486-12823_486-12822insGGTGGCCG
XM_017005413.1:c.*23-50215_*23-50214insGGTGGCCG (ACYP2)	XP_016860902.1:n.*23-50215_*23-50214insGGTGGCCG
XR_001739083.1:n.1092+31390_1092+31391insGGTGGCCG (ACYP2)
NM_001003937.3:c.*445_*446insCGGCCACC (TSPYL6) MANE Select	NP_001003937.2:n.*445_*446insCGGCCACC
NM_001320586.2:c.405-50215_405-50214insGGTGGCCG (ACYP2)	NP_001307515.1:n.405-50215_405-50214insGGTGGCCG
NM_001320587.2:c.312-50215_312-50214insGGTGGCCG (ACYP2)	NP_001307516.1:n.312-50215_312-50214insGGTGGCCG
NM_001320588.2:c.114-50215_114-50214insGGTGGCCG (ACYP2)	NP_001307517.1:n.114-50215_114-50214insGGTGGCCG
NM_001320589.2:c.186-12823_186-12822insGGTGGCCG (ACYP2)	NP_001307518.1:n.186-12823_186-12822insGGTGGCCG
NM_138448.4:c.186-50215_186-50214insGGTGGCCG (ACYP2) MANE Select	NP_612457.1:n.186-50215_186-50214insGGTGGCCG