Canonical Allele Identifier: CA1251655950

Gene: ACYP2 TSPYL6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254387_54254388delinsAG , CM000664.2:g.54254387_54254388delinsAG	GRCh38
NC_000002.11:g.54481524_54481525delinsAG , CM000664.1:g.54481524_54481525delinsAG	GRCh37
NC_000002.10:g.54335028_54335029delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50301_186-50300delinsAG (ACYP2) MANE Select	ENSP00000378161.3:n.186-50301_186-50300delinsAG
ENST00000394666.8:c.186-50301_186-50300delinsAG (ACYP2)	ENSP00000378161.3:n.186-50301_186-50300delinsAG
ENST00000317802.9:c.*531_*532delinsCT (TSPYL6) MANE Select	ENSP00000417919.2:n.*531_*532delinsCT
ENST00000607452.6:c.405-50301_405-50300delinsAG (ACYP2)	ENSP00000475986.1:n.405-50301_405-50300delinsAG
ENST00000303536.8:c.270-12909_270-12908delinsAG (ACYP2)	ENSP00000306448.4:n.270-12909_270-12908delinsAG
ENST00000317802.8:c.*531_*532delinsCT (TSPYL6)	ENSP00000417919.2:n.*531_*532delinsCT
ENST00000394666.7:c.186-50301_186-50300delinsAG (ACYP2)	ENSP00000378161.3:n.186-50301_186-50300delinsAG
ENST00000494922.6:c.265+31304_265+31305delinsAG (ACYP2)
ENST00000606865.1:c.138-50301_138-50300delinsAG (ACYP2)	ENSP00000475333.1:n.138-50301_138-50300delinsAG
ENST00000607452.5:c.405-50301_405-50300delinsAG (ACYP2)	ENSP00000475986.1:n.405-50301_405-50300delinsAG
NM_001003937.2:c.*531_*532delinsCT (TSPYL6)	NP_001003937.2:n.*531_*532delinsCT
NM_138448.3:c.186-50301_186-50300delinsAG (ACYP2)	NP_612457.1:n.186-50301_186-50300delinsAG
NM_001320586.1:c.405-50301_405-50300delinsAG (ACYP2)	NP_001307515.1:n.405-50301_405-50300delinsAG
NM_001320587.1:c.312-50301_312-50300delinsAG (ACYP2)	NP_001307516.1:n.312-50301_312-50300delinsAG
NM_001320588.1:c.114-50301_114-50300delinsAG (ACYP2)	NP_001307517.1:n.114-50301_114-50300delinsAG
NM_001320589.1:c.186-12909_186-12908delinsAG (ACYP2)	NP_001307518.1:n.186-12909_186-12908delinsAG
XM_017005411.1:c.486-50301_486-50300delinsAG (ACYP2)	XP_016860900.1:n.486-50301_486-50300delinsAG
XM_017005412.1:c.486-12909_486-12908delinsAG (ACYP2)	XP_016860901.1:n.486-12909_486-12908delinsAG
XM_017005413.1:c.*23-50301_*23-50300delinsAG (ACYP2)	XP_016860902.1:n.*23-50301_*23-50300delinsAG
XR_001739083.1:n.1092+31304_1092+31305delinsAG (ACYP2)
NM_001003937.3:c.*531_*532delinsCT (TSPYL6) MANE Select	NP_001003937.2:n.*531_*532delinsCT
NM_001320586.2:c.405-50301_405-50300delinsAG (ACYP2)	NP_001307515.1:n.405-50301_405-50300delinsAG
NM_001320587.2:c.312-50301_312-50300delinsAG (ACYP2)	NP_001307516.1:n.312-50301_312-50300delinsAG
NM_001320588.2:c.114-50301_114-50300delinsAG (ACYP2)	NP_001307517.1:n.114-50301_114-50300delinsAG
NM_001320589.2:c.186-12909_186-12908delinsAG (ACYP2)	NP_001307518.1:n.186-12909_186-12908delinsAG
NM_138448.4:c.186-50301_186-50300delinsAG (ACYP2) MANE Select	NP_612457.1:n.186-50301_186-50300delinsAG