Canonical Allele Identifier: CA2659051875

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254414-C-CGCCGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254414_54254415insGCCGTA , CM000664.2:g.54254414_54254415insGCCGTA	GRCh38
NC_000002.11:g.54481551_54481552insGCCGTA , CM000664.1:g.54481551_54481552insGCCGTA	GRCh37
NC_000002.10:g.54335055_54335056insGCCGTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50274_186-50273insGCCGTA (ACYP2) MANE Select	ENSP00000378161.3:n.186-50274_186-50273insGCCGTA
ENST00000394666.8:c.186-50274_186-50273insGCCGTA (ACYP2)	ENSP00000378161.3:n.186-50274_186-50273insGCCGTA
ENST00000317802.9:c.*504_*505insTACGGC (TSPYL6) MANE Select	ENSP00000417919.2:n.*504_*505insTACGGC
ENST00000607452.6:c.405-50274_405-50273insGCCGTA (ACYP2)	ENSP00000475986.1:n.405-50274_405-50273insGCCGTA
ENST00000303536.8:c.270-12882_270-12881insGCCGTA (ACYP2)	ENSP00000306448.4:n.270-12882_270-12881insGCCGTA
ENST00000317802.8:c.*504_*505insTACGGC (TSPYL6)	ENSP00000417919.2:n.*504_*505insTACGGC
ENST00000394666.7:c.186-50274_186-50273insGCCGTA (ACYP2)	ENSP00000378161.3:n.186-50274_186-50273insGCCGTA
ENST00000494922.6:c.265+31331_265+31332insGCCGTA (ACYP2)
ENST00000606865.1:c.138-50274_138-50273insGCCGTA (ACYP2)	ENSP00000475333.1:n.138-50274_138-50273insGCCGTA
ENST00000607452.5:c.405-50274_405-50273insGCCGTA (ACYP2)	ENSP00000475986.1:n.405-50274_405-50273insGCCGTA
NM_001003937.2:c.*504_*505insTACGGC (TSPYL6)	NP_001003937.2:n.*504_*505insTACGGC
NM_138448.3:c.186-50274_186-50273insGCCGTA (ACYP2)	NP_612457.1:n.186-50274_186-50273insGCCGTA
NM_001320586.1:c.405-50274_405-50273insGCCGTA (ACYP2)	NP_001307515.1:n.405-50274_405-50273insGCCGTA
NM_001320587.1:c.312-50274_312-50273insGCCGTA (ACYP2)	NP_001307516.1:n.312-50274_312-50273insGCCGTA
NM_001320588.1:c.114-50274_114-50273insGCCGTA (ACYP2)	NP_001307517.1:n.114-50274_114-50273insGCCGTA
NM_001320589.1:c.186-12882_186-12881insGCCGTA (ACYP2)	NP_001307518.1:n.186-12882_186-12881insGCCGTA
XM_017005411.1:c.486-50274_486-50273insGCCGTA (ACYP2)	XP_016860900.1:n.486-50274_486-50273insGCCGTA
XM_017005412.1:c.486-12882_486-12881insGCCGTA (ACYP2)	XP_016860901.1:n.486-12882_486-12881insGCCGTA
XM_017005413.1:c.*23-50274_*23-50273insGCCGTA (ACYP2)	XP_016860902.1:n.*23-50274_*23-50273insGCCGTA
XR_001739083.1:n.1092+31331_1092+31332insGCCGTA (ACYP2)
NM_001003937.3:c.*504_*505insTACGGC (TSPYL6) MANE Select	NP_001003937.2:n.*504_*505insTACGGC
NM_001320586.2:c.405-50274_405-50273insGCCGTA (ACYP2)	NP_001307515.1:n.405-50274_405-50273insGCCGTA
NM_001320587.2:c.312-50274_312-50273insGCCGTA (ACYP2)	NP_001307516.1:n.312-50274_312-50273insGCCGTA
NM_001320588.2:c.114-50274_114-50273insGCCGTA (ACYP2)	NP_001307517.1:n.114-50274_114-50273insGCCGTA
NM_001320589.2:c.186-12882_186-12881insGCCGTA (ACYP2)	NP_001307518.1:n.186-12882_186-12881insGCCGTA
NM_138448.4:c.186-50274_186-50273insGCCGTA (ACYP2) MANE Select	NP_612457.1:n.186-50274_186-50273insGCCGTA