Canonical Allele Identifier: CA2659052163
Gene: ACYP2 HGNC NCBI
TSPYL6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.54254640_54254641del , CM000664.2:g.54254640_54254641del GRCh38
NC_000002.11:g.54481777_54481778del , CM000664.1:g.54481777_54481778del GRCh37
NC_000002.10:g.54335281_54335282del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394666.9:c.186-50048_186-50047del (ACYP2) MANE Select ENSP00000378161.3:n.186-50048_186-50047del
ENST00000394666.8:c.186-50048_186-50047del (ACYP2) ENSP00000378161.3:n.186-50048_186-50047del
ENST00000317802.9:c.*278_*279del (TSPYL6) MANE Select ENSP00000417919.2:n.*278_*279del
ENST00000607452.6:c.405-50048_405-50047del (ACYP2) ENSP00000475986.1:n.405-50048_405-50047del
ENST00000303536.8:c.270-12656_270-12655del (ACYP2) ENSP00000306448.4:n.270-12656_270-12655del
ENST00000317802.8:c.*278_*279del (TSPYL6) ENSP00000417919.2:n.*278_*279del
ENST00000394666.7:c.186-50048_186-50047del (ACYP2) ENSP00000378161.3:n.186-50048_186-50047del
ENST00000494922.6:c.265+31557_265+31558del (ACYP2)
ENST00000606865.1:c.138-50048_138-50047del (ACYP2) ENSP00000475333.1:n.138-50048_138-50047del
ENST00000607452.5:c.405-50048_405-50047del (ACYP2) ENSP00000475986.1:n.405-50048_405-50047del
NM_001003937.2:c.*278_*279del (TSPYL6) NP_001003937.2:n.*278_*279del
NM_138448.3:c.186-50048_186-50047del (ACYP2) NP_612457.1:n.186-50048_186-50047del
NM_001320586.1:c.405-50048_405-50047del (ACYP2) NP_001307515.1:n.405-50048_405-50047del
NM_001320587.1:c.312-50048_312-50047del (ACYP2) NP_001307516.1:n.312-50048_312-50047del
NM_001320588.1:c.114-50048_114-50047del (ACYP2) NP_001307517.1:n.114-50048_114-50047del
NM_001320589.1:c.186-12656_186-12655del (ACYP2) NP_001307518.1:n.186-12656_186-12655del
XM_017005411.1:c.486-50048_486-50047del (ACYP2) XP_016860900.1:n.486-50048_486-50047del
XM_017005412.1:c.486-12656_486-12655del (ACYP2) XP_016860901.1:n.486-12656_486-12655del
XM_017005413.1:c.*23-50048_*23-50047del (ACYP2) XP_016860902.1:n.*23-50048_*23-50047del
XR_001739083.1:n.1092+31557_1092+31558del (ACYP2)
NM_001003937.3:c.*278_*279del (TSPYL6) MANE Select NP_001003937.2:n.*278_*279del
NM_001320586.2:c.405-50048_405-50047del (ACYP2) NP_001307515.1:n.405-50048_405-50047del
NM_001320587.2:c.312-50048_312-50047del (ACYP2) NP_001307516.1:n.312-50048_312-50047del
NM_001320588.2:c.114-50048_114-50047del (ACYP2) NP_001307517.1:n.114-50048_114-50047del
NM_001320589.2:c.186-12656_186-12655del (ACYP2) NP_001307518.1:n.186-12656_186-12655del
NM_138448.4:c.186-50048_186-50047del (ACYP2) MANE Select NP_612457.1:n.186-50048_186-50047del