Canonical Allele Identifier: CA2565365105

Gene: ACYP2 TSPYL6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254241_54254242insAGACCCTATCCTCATGGCAAGG , CM000664.2:g.54254241_54254242insAGACCCTATCCTCATGGCAAGG	GRCh38
NC_000002.11:g.54481378_54481379insAGACCCTATCCTCATGGCAAGG , CM000664.1:g.54481378_54481379insAGACCCTATCCTCATGGCAAGG	GRCh37
NC_000002.10:g.54334882_54334883insAGACCCTATCCTCATGGCAAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG (ACYP2) MANE Select	ENSP00000378161.3:n.186-50447_186-50446insAGACCCTATCCTCATGGCA...
ENST00000394666.8:c.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	ENSP00000378161.3:n.186-50447_186-50446insAGACCCTATCCTCATGGCA...
ENST00000317802.9:c.*677_*678insCCTTGCCATGAGGATAGGGTCT (TSPYL6) MANE Select	ENSP00000417919.2:n.*677_*678insCCTTGCCATGAGGATAGGGTCT
ENST00000607452.6:c.405-50447_405-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	ENSP00000475986.1:n.405-50447_405-50446insAGACCCTATCCTCATGGCA...
ENST00000303536.8:c.270-13055_270-13054insAGACCCTATCCTCATGGCAAGG (ACYP2)	ENSP00000306448.4:n.270-13055_270-13054insAGACCCTATCCTCATGGCA...
ENST00000317802.8:c.*677_*678insCCTTGCCATGAGGATAGGGTCT (TSPYL6)	ENSP00000417919.2:n.*677_*678insCCTTGCCATGAGGATAGGGTCT
ENST00000394666.7:c.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	ENSP00000378161.3:n.186-50447_186-50446insAGACCCTATCCTCATGGCA...
ENST00000494922.6:c.265+31158_265+31159insAGACCCTATCCTCATGGCAAGG (ACYP2)
ENST00000606865.1:c.138-50447_138-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	ENSP00000475333.1:n.138-50447_138-50446insAGACCCTATCCTCATGGCA...
ENST00000607452.5:c.405-50447_405-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	ENSP00000475986.1:n.405-50447_405-50446insAGACCCTATCCTCATGGCA...
NM_001003937.2:c.*677_*678insCCTTGCCATGAGGATAGGGTCT (TSPYL6)	NP_001003937.2:n.*677_*678insCCTTGCCATGAGGATAGGGTCT
NM_138448.3:c.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_612457.1:n.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG
NM_001320586.1:c.405-50447_405-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307515.1:n.405-50447_405-50446insAGACCCTATCCTCATGGCAAGG...
NM_001320587.1:c.312-50447_312-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307516.1:n.312-50447_312-50446insAGACCCTATCCTCATGGCAAGG...
NM_001320588.1:c.114-50447_114-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307517.1:n.114-50447_114-50446insAGACCCTATCCTCATGGCAAGG...
NM_001320589.1:c.186-13055_186-13054insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307518.1:n.186-13055_186-13054insAGACCCTATCCTCATGGCAAGG...
XM_017005411.1:c.486-50447_486-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	XP_016860900.1:n.486-50447_486-50446insAGACCCTATCCTCATGGCAAGG...
XM_017005412.1:c.486-13055_486-13054insAGACCCTATCCTCATGGCAAGG (ACYP2)	XP_016860901.1:n.486-13055_486-13054insAGACCCTATCCTCATGGCAAGG...
XM_017005413.1:c.*23-50447_*23-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	XP_016860902.1:n.*23-50447_*23-50446insAGACCCTATCCTCATGGCAAGG...
XR_001739083.1:n.1092+31158_1092+31159insAGACCCTATCCTCATGGCAAGG (ACYP2)
NM_001003937.3:c.*677_*678insCCTTGCCATGAGGATAGGGTCT (TSPYL6) MANE Select	NP_001003937.2:n.*677_*678insCCTTGCCATGAGGATAGGGTCT
NM_001320586.2:c.405-50447_405-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307515.1:n.405-50447_405-50446insAGACCCTATCCTCATGGCAAGG...
NM_001320587.2:c.312-50447_312-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307516.1:n.312-50447_312-50446insAGACCCTATCCTCATGGCAAGG...
NM_001320588.2:c.114-50447_114-50446insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307517.1:n.114-50447_114-50446insAGACCCTATCCTCATGGCAAGG...
NM_001320589.2:c.186-13055_186-13054insAGACCCTATCCTCATGGCAAGG (ACYP2)	NP_001307518.1:n.186-13055_186-13054insAGACCCTATCCTCATGGCAAGG...
NM_138448.4:c.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG (ACYP2) MANE Select	NP_612457.1:n.186-50447_186-50446insAGACCCTATCCTCATGGCAAGG