Canonical Allele Identifier: CA2659052151

Gene: ACYP2 TSPYL6

Linked Data

• gnomAD v4: 2-54254629-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254629A>C , CM000664.2:g.54254629A>C	GRCh38
NC_000002.11:g.54481766A>C , CM000664.1:g.54481766A>C	GRCh37
NC_000002.10:g.54335270A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394666.9:c.186-50059A>C (ACYP2) MANE Select	ENSP00000378161.3:n.186-50059A>C
ENST00000394666.8:c.186-50059A>C (ACYP2)	ENSP00000378161.3:n.186-50059A>C
ENST00000317802.9:c.*290T>G (TSPYL6) MANE Select	ENSP00000417919.2:n.*290T>G
ENST00000607452.6:c.405-50059A>C (ACYP2)	ENSP00000475986.1:n.405-50059A>C
ENST00000303536.8:c.270-12667A>C (ACYP2)	ENSP00000306448.4:n.270-12667A>C
ENST00000317802.8:c.*290T>G (TSPYL6)	ENSP00000417919.2:n.*290T>G
ENST00000394666.7:c.186-50059A>C (ACYP2)	ENSP00000378161.3:n.186-50059A>C
ENST00000494922.6:c.265+31546A>C (ACYP2)
ENST00000606865.1:c.138-50059A>C (ACYP2)	ENSP00000475333.1:n.138-50059A>C
ENST00000607452.5:c.405-50059A>C (ACYP2)	ENSP00000475986.1:n.405-50059A>C
NM_001003937.2:c.*290T>G (TSPYL6)	NP_001003937.2:n.*290T>G
NM_138448.3:c.186-50059A>C (ACYP2)	NP_612457.1:n.186-50059A>C
NM_001320586.1:c.405-50059A>C (ACYP2)	NP_001307515.1:n.405-50059A>C
NM_001320587.1:c.312-50059A>C (ACYP2)	NP_001307516.1:n.312-50059A>C
NM_001320588.1:c.114-50059A>C (ACYP2)	NP_001307517.1:n.114-50059A>C
NM_001320589.1:c.186-12667A>C (ACYP2)	NP_001307518.1:n.186-12667A>C
XM_017005411.1:c.486-50059A>C (ACYP2)	XP_016860900.1:n.486-50059A>C
XM_017005412.1:c.486-12667A>C (ACYP2)	XP_016860901.1:n.486-12667A>C
XM_017005413.1:c.*23-50059A>C (ACYP2)	XP_016860902.1:n.*23-50059A>C
XR_001739083.1:n.1092+31546A>C (ACYP2)
NM_001003937.3:c.*290T>G (TSPYL6) MANE Select	NP_001003937.2:n.*290T>G
NM_001320586.2:c.405-50059A>C (ACYP2)	NP_001307515.1:n.405-50059A>C
NM_001320587.2:c.312-50059A>C (ACYP2)	NP_001307516.1:n.312-50059A>C
NM_001320588.2:c.114-50059A>C (ACYP2)	NP_001307517.1:n.114-50059A>C
NM_001320589.2:c.186-12667A>C (ACYP2)	NP_001307518.1:n.186-12667A>C
NM_138448.4:c.186-50059A>C (ACYP2) MANE Select	NP_612457.1:n.186-50059A>C