Canonical Allele Identifier: CA770168560

Gene: ACYP2 TSPYL6

Linked Data

• dbSNP Id: rs1406868215
• gnomAD v3: 2-54254272-C-T
• gnomAD v4: 2-54254272-C-T
• MyVariant Identifiers: chr2:g.54481409C>T (hg19) ; chr2:g.54254272C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254272C>T , CM000664.2:g.54254272C>T	GRCh38
NC_000002.11:g.54481409C>T , CM000664.1:g.54481409C>T	GRCh37
NC_000002.10:g.54334913C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394666.9:c.186-50416C>T (ACYP2) MANE Select	ENSP00000378161.3:n.186-50416C>T
ENST00000394666.8:c.186-50416C>T (ACYP2)	ENSP00000378161.3:n.186-50416C>T
ENST00000317802.9:c.*647G>A (TSPYL6) MANE Select	ENSP00000417919.2:n.*647G>A
ENST00000607452.6:c.405-50416C>T (ACYP2)	ENSP00000475986.1:n.405-50416C>T
ENST00000303536.8:c.270-13024C>T (ACYP2)	ENSP00000306448.4:n.270-13024C>T
ENST00000317802.8:c.*647G>A (TSPYL6)	ENSP00000417919.2:n.*647G>A
ENST00000394666.7:c.186-50416C>T (ACYP2)	ENSP00000378161.3:n.186-50416C>T
ENST00000494922.6:c.265+31189C>T (ACYP2)
ENST00000606865.1:c.138-50416C>T (ACYP2)	ENSP00000475333.1:n.138-50416C>T
ENST00000607452.5:c.405-50416C>T (ACYP2)	ENSP00000475986.1:n.405-50416C>T
NM_001003937.2:c.*647G>A (TSPYL6)	NP_001003937.2:n.*647G>A
NM_138448.3:c.186-50416C>T (ACYP2)	NP_612457.1:n.186-50416C>T
NM_001320586.1:c.405-50416C>T (ACYP2)	NP_001307515.1:n.405-50416C>T
NM_001320587.1:c.312-50416C>T (ACYP2)	NP_001307516.1:n.312-50416C>T
NM_001320588.1:c.114-50416C>T (ACYP2)	NP_001307517.1:n.114-50416C>T
NM_001320589.1:c.186-13024C>T (ACYP2)	NP_001307518.1:n.186-13024C>T
XM_017005411.1:c.486-50416C>T (ACYP2)	XP_016860900.1:n.486-50416C>T
XM_017005412.1:c.486-13024C>T (ACYP2)	XP_016860901.1:n.486-13024C>T
XM_017005413.1:c.*23-50416C>T (ACYP2)	XP_016860902.1:n.*23-50416C>T
XR_001739083.1:n.1092+31189C>T (ACYP2)
NM_001003937.3:c.*647G>A (TSPYL6) MANE Select	NP_001003937.2:n.*647G>A
NM_001320586.2:c.405-50416C>T (ACYP2)	NP_001307515.1:n.405-50416C>T
NM_001320587.2:c.312-50416C>T (ACYP2)	NP_001307516.1:n.312-50416C>T
NM_001320588.2:c.114-50416C>T (ACYP2)	NP_001307517.1:n.114-50416C>T
NM_001320589.2:c.186-13024C>T (ACYP2)	NP_001307518.1:n.186-13024C>T
NM_138448.4:c.186-50416C>T (ACYP2) MANE Select	NP_612457.1:n.186-50416C>T