Canonical Allele Identifier: CA47485280

Gene: ACYP2 TSPYL6

Linked Data

• dbSNP Id: rs1021211375
• MyVariant Identifiers: chr2:g.54481549G>C (hg19) ; chr2:g.54254412G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54254412G>C , CM000664.2:g.54254412G>C	GRCh38
NC_000002.11:g.54481549G>C , CM000664.1:g.54481549G>C	GRCh37
NC_000002.10:g.54335053G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394666.9:c.186-50276G>C (ACYP2) MANE Select	ENSP00000378161.3:n.186-50276G>C
ENST00000394666.8:c.186-50276G>C (ACYP2)	ENSP00000378161.3:n.186-50276G>C
ENST00000317802.9:c.*507C>G (TSPYL6) MANE Select	ENSP00000417919.2:n.*507C>G
ENST00000607452.6:c.405-50276G>C (ACYP2)	ENSP00000475986.1:n.405-50276G>C
ENST00000303536.8:c.270-12884G>C (ACYP2)	ENSP00000306448.4:n.270-12884G>C
ENST00000317802.8:c.*507C>G (TSPYL6)	ENSP00000417919.2:n.*507C>G
ENST00000394666.7:c.186-50276G>C (ACYP2)	ENSP00000378161.3:n.186-50276G>C
ENST00000494922.6:c.265+31329G>C (ACYP2)
ENST00000606865.1:c.138-50276G>C (ACYP2)	ENSP00000475333.1:n.138-50276G>C
ENST00000607452.5:c.405-50276G>C (ACYP2)	ENSP00000475986.1:n.405-50276G>C
NM_001003937.2:c.*507C>G (TSPYL6)	NP_001003937.2:n.*507C>G
NM_138448.3:c.186-50276G>C (ACYP2)	NP_612457.1:n.186-50276G>C
NM_001320586.1:c.405-50276G>C (ACYP2)	NP_001307515.1:n.405-50276G>C
NM_001320587.1:c.312-50276G>C (ACYP2)	NP_001307516.1:n.312-50276G>C
NM_001320588.1:c.114-50276G>C (ACYP2)	NP_001307517.1:n.114-50276G>C
NM_001320589.1:c.186-12884G>C (ACYP2)	NP_001307518.1:n.186-12884G>C
XM_017005411.1:c.486-50276G>C (ACYP2)	XP_016860900.1:n.486-50276G>C
XM_017005412.1:c.486-12884G>C (ACYP2)	XP_016860901.1:n.486-12884G>C
XM_017005413.1:c.*23-50276G>C (ACYP2)	XP_016860902.1:n.*23-50276G>C
XR_001739083.1:n.1092+31329G>C (ACYP2)
NM_001003937.3:c.*507C>G (TSPYL6) MANE Select	NP_001003937.2:n.*507C>G
NM_001320586.2:c.405-50276G>C (ACYP2)	NP_001307515.1:n.405-50276G>C
NM_001320587.2:c.312-50276G>C (ACYP2)	NP_001307516.1:n.312-50276G>C
NM_001320588.2:c.114-50276G>C (ACYP2)	NP_001307517.1:n.114-50276G>C
NM_001320589.2:c.186-12884G>C (ACYP2)	NP_001307518.1:n.186-12884G>C
NM_138448.4:c.186-50276G>C (ACYP2) MANE Select	NP_612457.1:n.186-50276G>C