Canonical Allele Identifier: CA2659052175

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254651-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254652_54254653del , CM000664.2:g.54254652_54254653del	GRCh38
NC_000002.11:g.54481789_54481790del , CM000664.1:g.54481789_54481790del	GRCh37
NC_000002.10:g.54335293_54335294del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50036_186-50035del (ACYP2) MANE Select	ENSP00000378161.3:n.186-50036_186-50035del
ENST00000394666.8:c.186-50036_186-50035del (ACYP2)	ENSP00000378161.3:n.186-50036_186-50035del
ENST00000317802.9:c.*266_*267del (TSPYL6) MANE Select	ENSP00000417919.2:n.*266_*267del
ENST00000607452.6:c.405-50036_405-50035del (ACYP2)	ENSP00000475986.1:n.405-50036_405-50035del
ENST00000303536.8:c.270-12644_270-12643del (ACYP2)	ENSP00000306448.4:n.270-12644_270-12643del
ENST00000317802.8:c.*266_*267del (TSPYL6)	ENSP00000417919.2:n.*266_*267del
ENST00000394666.7:c.186-50036_186-50035del (ACYP2)	ENSP00000378161.3:n.186-50036_186-50035del
ENST00000494922.6:c.265+31569_265+31570del (ACYP2)
ENST00000606865.1:c.138-50036_138-50035del (ACYP2)	ENSP00000475333.1:n.138-50036_138-50035del
ENST00000607452.5:c.405-50036_405-50035del (ACYP2)	ENSP00000475986.1:n.405-50036_405-50035del
NM_001003937.2:c.*266_*267del (TSPYL6)	NP_001003937.2:n.*266_*267del
NM_138448.3:c.186-50036_186-50035del (ACYP2)	NP_612457.1:n.186-50036_186-50035del
NM_001320586.1:c.405-50036_405-50035del (ACYP2)	NP_001307515.1:n.405-50036_405-50035del
NM_001320587.1:c.312-50036_312-50035del (ACYP2)	NP_001307516.1:n.312-50036_312-50035del
NM_001320588.1:c.114-50036_114-50035del (ACYP2)	NP_001307517.1:n.114-50036_114-50035del
NM_001320589.1:c.186-12644_186-12643del (ACYP2)	NP_001307518.1:n.186-12644_186-12643del
XM_017005411.1:c.486-50036_486-50035del (ACYP2)	XP_016860900.1:n.486-50036_486-50035del
XM_017005412.1:c.486-12644_486-12643del (ACYP2)	XP_016860901.1:n.486-12644_486-12643del
XM_017005413.1:c.*23-50036_*23-50035del (ACYP2)	XP_016860902.1:n.*23-50036_*23-50035del
XR_001739083.1:n.1092+31569_1092+31570del (ACYP2)
NM_001003937.3:c.*266_*267del (TSPYL6) MANE Select	NP_001003937.2:n.*266_*267del
NM_001320586.2:c.405-50036_405-50035del (ACYP2)	NP_001307515.1:n.405-50036_405-50035del
NM_001320587.2:c.312-50036_312-50035del (ACYP2)	NP_001307516.1:n.312-50036_312-50035del
NM_001320588.2:c.114-50036_114-50035del (ACYP2)	NP_001307517.1:n.114-50036_114-50035del
NM_001320589.2:c.186-12644_186-12643del (ACYP2)	NP_001307518.1:n.186-12644_186-12643del
NM_138448.4:c.186-50036_186-50035del (ACYP2) MANE Select	NP_612457.1:n.186-50036_186-50035del