Canonical Allele Identifier: CA1251656098

Gene: ACYP2 TSPYL6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254672_54254673delinsGA , CM000664.2:g.54254672_54254673delinsGA	GRCh38
NC_000002.11:g.54481809_54481810delinsGA , CM000664.1:g.54481809_54481810delinsGA	GRCh37
NC_000002.10:g.54335313_54335314delinsGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50016_186-50015delinsGA (ACYP2) MANE Select	ENSP00000378161.3:n.186-50016_186-50015delinsGA
ENST00000394666.8:c.186-50016_186-50015delinsGA (ACYP2)	ENSP00000378161.3:n.186-50016_186-50015delinsGA
ENST00000317802.9:c.*246_*247delinsTC (TSPYL6) MANE Select	ENSP00000417919.2:n.*246_*247delinsTC
ENST00000607452.6:c.405-50016_405-50015delinsGA (ACYP2)	ENSP00000475986.1:n.405-50016_405-50015delinsGA
ENST00000303536.8:c.270-12624_270-12623delinsGA (ACYP2)	ENSP00000306448.4:n.270-12624_270-12623delinsGA
ENST00000317802.8:c.*246_*247delinsTC (TSPYL6)	ENSP00000417919.2:n.*246_*247delinsTC
ENST00000394666.7:c.186-50016_186-50015delinsGA (ACYP2)	ENSP00000378161.3:n.186-50016_186-50015delinsGA
ENST00000494922.6:c.265+31589_265+31590delinsGA (ACYP2)
ENST00000606865.1:c.138-50016_138-50015delinsGA (ACYP2)	ENSP00000475333.1:n.138-50016_138-50015delinsGA
ENST00000607452.5:c.405-50016_405-50015delinsGA (ACYP2)	ENSP00000475986.1:n.405-50016_405-50015delinsGA
NM_001003937.2:c.*246_*247delinsTC (TSPYL6)	NP_001003937.2:n.*246_*247delinsTC
NM_138448.3:c.186-50016_186-50015delinsGA (ACYP2)	NP_612457.1:n.186-50016_186-50015delinsGA
NM_001320586.1:c.405-50016_405-50015delinsGA (ACYP2)	NP_001307515.1:n.405-50016_405-50015delinsGA
NM_001320587.1:c.312-50016_312-50015delinsGA (ACYP2)	NP_001307516.1:n.312-50016_312-50015delinsGA
NM_001320588.1:c.114-50016_114-50015delinsGA (ACYP2)	NP_001307517.1:n.114-50016_114-50015delinsGA
NM_001320589.1:c.186-12624_186-12623delinsGA (ACYP2)	NP_001307518.1:n.186-12624_186-12623delinsGA
XM_017005411.1:c.486-50016_486-50015delinsGA (ACYP2)	XP_016860900.1:n.486-50016_486-50015delinsGA
XM_017005412.1:c.486-12624_486-12623delinsGA (ACYP2)	XP_016860901.1:n.486-12624_486-12623delinsGA
XM_017005413.1:c.*23-50016_*23-50015delinsGA (ACYP2)	XP_016860902.1:n.*23-50016_*23-50015delinsGA
XR_001739083.1:n.1092+31589_1092+31590delinsGA (ACYP2)
NM_001003937.3:c.*246_*247delinsTC (TSPYL6) MANE Select	NP_001003937.2:n.*246_*247delinsTC
NM_001320586.2:c.405-50016_405-50015delinsGA (ACYP2)	NP_001307515.1:n.405-50016_405-50015delinsGA
NM_001320587.2:c.312-50016_312-50015delinsGA (ACYP2)	NP_001307516.1:n.312-50016_312-50015delinsGA
NM_001320588.2:c.114-50016_114-50015delinsGA (ACYP2)	NP_001307517.1:n.114-50016_114-50015delinsGA
NM_001320589.2:c.186-12624_186-12623delinsGA (ACYP2)	NP_001307518.1:n.186-12624_186-12623delinsGA
NM_138448.4:c.186-50016_186-50015delinsGA (ACYP2) MANE Select	NP_612457.1:n.186-50016_186-50015delinsGA