Canonical Allele Identifier: CA15186551
Gene: TSPYL6 HGNC NCBI
ACYP2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10165485

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.54254499T>C , CM000664.2:g.54254499T>C GRCh38
NC_000002.11:g.54481636T>C , CM000664.1:g.54481636T>C GRCh37
NC_000002.10:g.54335140T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001003937.2:c.*420A>G (TSPYL6) VV NP_001003937.2:p.=
NM_138448.3:c.186-50189T>C (ACYP2) VV NP_612457.1:p.=
NM_001320586.1:c.405-50189T>C (ACYP2) VV NP_001307515.1:p.=
NM_001320587.1:c.312-50189T>C (ACYP2) VV NP_001307516.1:p.=
NM_001320588.1:c.114-50189T>C (ACYP2) VV NP_001307517.1:p.=
NM_001320589.1:c.186-12797T>C (ACYP2) VV NP_001307518.1:p.=
XM_017005411.1:c.486-50189T>C (ACYP2) XP_016860900.1:p.=
XM_017005412.1:c.486-12797T>C (ACYP2) XP_016860901.1:p.=
XM_017005413.1:c.*23-50189T>C (ACYP2) XP_016860902.1:p.=
XR_001739083.1:n.1092+31416T>C (ACYP2)
ENST00000303536.8:c.270-12797T>C ENSP00000306448.4:p.=
ENST00000317802.8:c.*420A>G ENSP00000417919.2:p.=
ENST00000394666.7:c.186-50189T>C ENSP00000378161.3:p.=
ENST00000494922.6:n.265+31416T>C
ENST00000606865.1:c.138-50189T>C ENSP00000475333.1:p.=
ENST00000607452.5:c.405-50189T>C ENSP00000475986.1:p.=