Canonical Allele Identifier: CA2659052052

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254524-T-TGACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254525_54254526insACAGG , CM000664.2:g.54254525_54254526insACAGG	GRCh38
NC_000002.11:g.54481662_54481663insACAGG , CM000664.1:g.54481662_54481663insACAGG	GRCh37
NC_000002.10:g.54335166_54335167insACAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50163_186-50162insACAGG (ACYP2) MANE Select	ENSP00000378161.3:n.186-50163_186-50162insACAGG
ENST00000394666.8:c.186-50163_186-50162insACAGG (ACYP2)	ENSP00000378161.3:n.186-50163_186-50162insACAGG
ENST00000317802.9:c.*394_*395insCTGTC (TSPYL6) MANE Select	ENSP00000417919.2:n.*394_*395insCTGTC
ENST00000607452.6:c.405-50163_405-50162insACAGG (ACYP2)	ENSP00000475986.1:n.405-50163_405-50162insACAGG
ENST00000303536.8:c.270-12771_270-12770insACAGG (ACYP2)	ENSP00000306448.4:n.270-12771_270-12770insACAGG
ENST00000317802.8:c.*394_*395insCTGTC (TSPYL6)	ENSP00000417919.2:n.*394_*395insCTGTC
ENST00000394666.7:c.186-50163_186-50162insACAGG (ACYP2)	ENSP00000378161.3:n.186-50163_186-50162insACAGG
ENST00000494922.6:c.265+31442_265+31443insACAGG (ACYP2)
ENST00000606865.1:c.138-50163_138-50162insACAGG (ACYP2)	ENSP00000475333.1:n.138-50163_138-50162insACAGG
ENST00000607452.5:c.405-50163_405-50162insACAGG (ACYP2)	ENSP00000475986.1:n.405-50163_405-50162insACAGG
NM_001003937.2:c.*394_*395insCTGTC (TSPYL6)	NP_001003937.2:n.*394_*395insCTGTC
NM_138448.3:c.186-50163_186-50162insACAGG (ACYP2)	NP_612457.1:n.186-50163_186-50162insACAGG
NM_001320586.1:c.405-50163_405-50162insACAGG (ACYP2)	NP_001307515.1:n.405-50163_405-50162insACAGG
NM_001320587.1:c.312-50163_312-50162insACAGG (ACYP2)	NP_001307516.1:n.312-50163_312-50162insACAGG
NM_001320588.1:c.114-50163_114-50162insACAGG (ACYP2)	NP_001307517.1:n.114-50163_114-50162insACAGG
NM_001320589.1:c.186-12771_186-12770insACAGG (ACYP2)	NP_001307518.1:n.186-12771_186-12770insACAGG
XM_017005411.1:c.486-50163_486-50162insACAGG (ACYP2)	XP_016860900.1:n.486-50163_486-50162insACAGG
XM_017005412.1:c.486-12771_486-12770insACAGG (ACYP2)	XP_016860901.1:n.486-12771_486-12770insACAGG
XM_017005413.1:c.*23-50163_*23-50162insACAGG (ACYP2)	XP_016860902.1:n.*23-50163_*23-50162insACAGG
XR_001739083.1:n.1092+31442_1092+31443insACAGG (ACYP2)
NM_001003937.3:c.*394_*395insCTGTC (TSPYL6) MANE Select	NP_001003937.2:n.*394_*395insCTGTC
NM_001320586.2:c.405-50163_405-50162insACAGG (ACYP2)	NP_001307515.1:n.405-50163_405-50162insACAGG
NM_001320587.2:c.312-50163_312-50162insACAGG (ACYP2)	NP_001307516.1:n.312-50163_312-50162insACAGG
NM_001320588.2:c.114-50163_114-50162insACAGG (ACYP2)	NP_001307517.1:n.114-50163_114-50162insACAGG
NM_001320589.2:c.186-12771_186-12770insACAGG (ACYP2)	NP_001307518.1:n.186-12771_186-12770insACAGG
NM_138448.4:c.186-50163_186-50162insACAGG (ACYP2) MANE Select	NP_612457.1:n.186-50163_186-50162insACAGG