Canonical Allele Identifier: CA2659052255

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254744-G-GATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254744_54254745insATCT , CM000664.2:g.54254744_54254745insATCT	GRCh38
NC_000002.11:g.54481881_54481882insATCT , CM000664.1:g.54481881_54481882insATCT	GRCh37
NC_000002.10:g.54335385_54335386insATCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-49944_186-49943insATCT (ACYP2) MANE Select	ENSP00000378161.3:n.186-49944_186-49943insATCT
ENST00000394666.8:c.186-49944_186-49943insATCT (ACYP2)	ENSP00000378161.3:n.186-49944_186-49943insATCT
ENST00000317802.9:c.*174_*175insAGAT (TSPYL6) MANE Select	ENSP00000417919.2:n.*174_*175insAGAT
ENST00000607452.6:c.405-49944_405-49943insATCT (ACYP2)	ENSP00000475986.1:n.405-49944_405-49943insATCT
ENST00000303536.8:c.270-12552_270-12551insATCT (ACYP2)	ENSP00000306448.4:n.270-12552_270-12551insATCT
ENST00000317802.8:c.*174_*175insAGAT (TSPYL6)	ENSP00000417919.2:n.*174_*175insAGAT
ENST00000394666.7:c.186-49944_186-49943insATCT (ACYP2)	ENSP00000378161.3:n.186-49944_186-49943insATCT
ENST00000494922.6:c.265+31661_265+31662insATCT (ACYP2)
ENST00000606865.1:c.138-49944_138-49943insATCT (ACYP2)	ENSP00000475333.1:n.138-49944_138-49943insATCT
ENST00000607452.5:c.405-49944_405-49943insATCT (ACYP2)	ENSP00000475986.1:n.405-49944_405-49943insATCT
NM_001003937.2:c.*174_*175insAGAT (TSPYL6)	NP_001003937.2:n.*174_*175insAGAT
NM_138448.3:c.186-49944_186-49943insATCT (ACYP2)	NP_612457.1:n.186-49944_186-49943insATCT
NM_001320586.1:c.405-49944_405-49943insATCT (ACYP2)	NP_001307515.1:n.405-49944_405-49943insATCT
NM_001320587.1:c.312-49944_312-49943insATCT (ACYP2)	NP_001307516.1:n.312-49944_312-49943insATCT
NM_001320588.1:c.114-49944_114-49943insATCT (ACYP2)	NP_001307517.1:n.114-49944_114-49943insATCT
NM_001320589.1:c.186-12552_186-12551insATCT (ACYP2)	NP_001307518.1:n.186-12552_186-12551insATCT
XM_017005411.1:c.486-49944_486-49943insATCT (ACYP2)	XP_016860900.1:n.486-49944_486-49943insATCT
XM_017005412.1:c.486-12552_486-12551insATCT (ACYP2)	XP_016860901.1:n.486-12552_486-12551insATCT
XM_017005413.1:c.*23-49944_*23-49943insATCT (ACYP2)	XP_016860902.1:n.*23-49944_*23-49943insATCT
XR_001739083.1:n.1092+31661_1092+31662insATCT (ACYP2)
NM_001003937.3:c.*174_*175insAGAT (TSPYL6) MANE Select	NP_001003937.2:n.*174_*175insAGAT
NM_001320586.2:c.405-49944_405-49943insATCT (ACYP2)	NP_001307515.1:n.405-49944_405-49943insATCT
NM_001320587.2:c.312-49944_312-49943insATCT (ACYP2)	NP_001307516.1:n.312-49944_312-49943insATCT
NM_001320588.2:c.114-49944_114-49943insATCT (ACYP2)	NP_001307517.1:n.114-49944_114-49943insATCT
NM_001320589.2:c.186-12552_186-12551insATCT (ACYP2)	NP_001307518.1:n.186-12552_186-12551insATCT
NM_138448.4:c.186-49944_186-49943insATCT (ACYP2) MANE Select	NP_612457.1:n.186-49944_186-49943insATCT