Canonical Allele Identifier: CA2659051990

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254481-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254482_54254483insAT , CM000664.2:g.54254482_54254483insAT	GRCh38
NC_000002.11:g.54481619_54481620insAT , CM000664.1:g.54481619_54481620insAT	GRCh37
NC_000002.10:g.54335123_54335124insAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394666.9:c.186-50206_186-50205insAT (ACYP2) MANE Select	ENSP00000378161.3:n.186-50206_186-50205insAT
ENST00000394666.8:c.186-50206_186-50205insAT (ACYP2)	ENSP00000378161.3:n.186-50206_186-50205insAT
ENST00000317802.9:c.*437_*438insTA (TSPYL6) MANE Select	ENSP00000417919.2:n.*437_*438insTA
ENST00000607452.6:c.405-50206_405-50205insAT (ACYP2)	ENSP00000475986.1:n.405-50206_405-50205insAT
ENST00000303536.8:c.270-12814_270-12813insAT (ACYP2)	ENSP00000306448.4:n.270-12814_270-12813insAT
ENST00000317802.8:c.*437_*438insTA (TSPYL6)	ENSP00000417919.2:n.*437_*438insTA
ENST00000394666.7:c.186-50206_186-50205insAT (ACYP2)	ENSP00000378161.3:n.186-50206_186-50205insAT
ENST00000494922.6:c.265+31399_265+31400insAT (ACYP2)
ENST00000606865.1:c.138-50206_138-50205insAT (ACYP2)	ENSP00000475333.1:n.138-50206_138-50205insAT
ENST00000607452.5:c.405-50206_405-50205insAT (ACYP2)	ENSP00000475986.1:n.405-50206_405-50205insAT
NM_001003937.2:c.*437_*438insTA (TSPYL6)	NP_001003937.2:n.*437_*438insTA
NM_138448.3:c.186-50206_186-50205insAT (ACYP2)	NP_612457.1:n.186-50206_186-50205insAT
NM_001320586.1:c.405-50206_405-50205insAT (ACYP2)	NP_001307515.1:n.405-50206_405-50205insAT
NM_001320587.1:c.312-50206_312-50205insAT (ACYP2)	NP_001307516.1:n.312-50206_312-50205insAT
NM_001320588.1:c.114-50206_114-50205insAT (ACYP2)	NP_001307517.1:n.114-50206_114-50205insAT
NM_001320589.1:c.186-12814_186-12813insAT (ACYP2)	NP_001307518.1:n.186-12814_186-12813insAT
XM_017005411.1:c.486-50206_486-50205insAT (ACYP2)	XP_016860900.1:n.486-50206_486-50205insAT
XM_017005412.1:c.486-12814_486-12813insAT (ACYP2)	XP_016860901.1:n.486-12814_486-12813insAT
XM_017005413.1:c.*23-50206_*23-50205insAT (ACYP2)	XP_016860902.1:n.*23-50206_*23-50205insAT
XR_001739083.1:n.1092+31399_1092+31400insAT (ACYP2)
NM_001003937.3:c.*437_*438insTA (TSPYL6) MANE Select	NP_001003937.2:n.*437_*438insTA
NM_001320586.2:c.405-50206_405-50205insAT (ACYP2)	NP_001307515.1:n.405-50206_405-50205insAT
NM_001320587.2:c.312-50206_312-50205insAT (ACYP2)	NP_001307516.1:n.312-50206_312-50205insAT
NM_001320588.2:c.114-50206_114-50205insAT (ACYP2)	NP_001307517.1:n.114-50206_114-50205insAT
NM_001320589.2:c.186-12814_186-12813insAT (ACYP2)	NP_001307518.1:n.186-12814_186-12813insAT
NM_138448.4:c.186-50206_186-50205insAT (ACYP2) MANE Select	NP_612457.1:n.186-50206_186-50205insAT