Canonical Allele Identifier: CA2659052309

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254777-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254782_54254783del , CM000664.2:g.54254782_54254783del	GRCh38
NC_000002.11:g.54481919_54481920del , CM000664.1:g.54481919_54481920del	GRCh37
NC_000002.10:g.54335423_54335424del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-49906_186-49905del (ACYP2) MANE Select	ENSP00000378161.3:n.186-49906_186-49905del
ENST00000394666.8:c.186-49906_186-49905del (ACYP2)	ENSP00000378161.3:n.186-49906_186-49905del
ENST00000317802.9:c.*140_*141del (TSPYL6) MANE Select	ENSP00000417919.2:n.*140_*141del
ENST00000607452.6:c.405-49906_405-49905del (ACYP2)	ENSP00000475986.1:n.405-49906_405-49905del
ENST00000303536.8:c.270-12514_270-12513del (ACYP2)	ENSP00000306448.4:n.270-12514_270-12513del
ENST00000317802.8:c.*140_*141del (TSPYL6)	ENSP00000417919.2:n.*140_*141del
ENST00000394666.7:c.186-49906_186-49905del (ACYP2)	ENSP00000378161.3:n.186-49906_186-49905del
ENST00000494922.6:c.265+31699_265+31700del (ACYP2)
ENST00000606865.1:c.138-49906_138-49905del (ACYP2)	ENSP00000475333.1:n.138-49906_138-49905del
ENST00000607452.5:c.405-49906_405-49905del (ACYP2)	ENSP00000475986.1:n.405-49906_405-49905del
NM_001003937.2:c.*140_*141del (TSPYL6)	NP_001003937.2:n.*140_*141del
NM_138448.3:c.186-49906_186-49905del (ACYP2)	NP_612457.1:n.186-49906_186-49905del
NM_001320586.1:c.405-49906_405-49905del (ACYP2)	NP_001307515.1:n.405-49906_405-49905del
NM_001320587.1:c.312-49906_312-49905del (ACYP2)	NP_001307516.1:n.312-49906_312-49905del
NM_001320588.1:c.114-49906_114-49905del (ACYP2)	NP_001307517.1:n.114-49906_114-49905del
NM_001320589.1:c.186-12514_186-12513del (ACYP2)	NP_001307518.1:n.186-12514_186-12513del
XM_017005411.1:c.486-49906_486-49905del (ACYP2)	XP_016860900.1:n.486-49906_486-49905del
XM_017005412.1:c.486-12514_486-12513del (ACYP2)	XP_016860901.1:n.486-12514_486-12513del
XM_017005413.1:c.*23-49906_*23-49905del (ACYP2)	XP_016860902.1:n.*23-49906_*23-49905del
XR_001739083.1:n.1092+31699_1092+31700del (ACYP2)
NM_001003937.3:c.*140_*141del (TSPYL6) MANE Select	NP_001003937.2:n.*140_*141del
NM_001320586.2:c.405-49906_405-49905del (ACYP2)	NP_001307515.1:n.405-49906_405-49905del
NM_001320587.2:c.312-49906_312-49905del (ACYP2)	NP_001307516.1:n.312-49906_312-49905del
NM_001320588.2:c.114-49906_114-49905del (ACYP2)	NP_001307517.1:n.114-49906_114-49905del
NM_001320589.2:c.186-12514_186-12513del (ACYP2)	NP_001307518.1:n.186-12514_186-12513del
NM_138448.4:c.186-49906_186-49905del (ACYP2) MANE Select	NP_612457.1:n.186-49906_186-49905del