Canonical Allele Identifier: CA2659051814
Gene: ACYP2 HGNC NCBI
TSPYL6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.54254344_54254345del , CM000664.2:g.54254344_54254345del GRCh38
NC_000002.11:g.54481481_54481482del , CM000664.1:g.54481481_54481482del GRCh37
NC_000002.10:g.54334985_54334986del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394666.9:c.186-50344_186-50343del (ACYP2) MANE Select ENSP00000378161.3:n.186-50344_186-50343de...
ENST00000394666.8:c.186-50344_186-50343del (ACYP2) ENSP00000378161.3:n.186-50344_186-50343de...
ENST00000317802.9:c.*575_*576del (TSPYL6) MANE Select ENSP00000417919.2:n.*575_*576del
ENST00000607452.6:c.405-50344_405-50343del (ACYP2) ENSP00000475986.1:n.405-50344_405-50343de...
ENST00000303536.8:c.270-12952_270-12951del (ACYP2) ENSP00000306448.4:n.270-12952_270-12951de...
ENST00000317802.8:c.*575_*576del (TSPYL6) ENSP00000417919.2:n.*575_*576del
ENST00000394666.7:c.186-50344_186-50343del (ACYP2) ENSP00000378161.3:n.186-50344_186-50343de...
ENST00000494922.6:c.265+31261_265+31262del (ACYP2)
ENST00000606865.1:c.138-50344_138-50343del (ACYP2) ENSP00000475333.1:n.138-50344_138-50343de...
ENST00000607452.5:c.405-50344_405-50343del (ACYP2) ENSP00000475986.1:n.405-50344_405-50343de...
NM_001003937.2:c.*575_*576del (TSPYL6) NP_001003937.2:n.*575_*576del
NM_138448.3:c.186-50344_186-50343del (ACYP2) NP_612457.1:n.186-50344_186-50343del
NM_001320586.1:c.405-50344_405-50343del (ACYP2) NP_001307515.1:n.405-50344_405-50343del
NM_001320587.1:c.312-50344_312-50343del (ACYP2) NP_001307516.1:n.312-50344_312-50343del
NM_001320588.1:c.114-50344_114-50343del (ACYP2) NP_001307517.1:n.114-50344_114-50343del
NM_001320589.1:c.186-12952_186-12951del (ACYP2) NP_001307518.1:n.186-12952_186-12951del
XM_017005411.1:c.486-50344_486-50343del (ACYP2) XP_016860900.1:n.486-50344_486-50343del
XM_017005412.1:c.486-12952_486-12951del (ACYP2) XP_016860901.1:n.486-12952_486-12951del
XM_017005413.1:c.*23-50344_*23-50343del (ACYP2) XP_016860902.1:n.*23-50344_*23-50343del
XR_001739083.1:n.1092+31261_1092+31262del (ACYP2)
NM_001003937.3:c.*575_*576del (TSPYL6) MANE Select NP_001003937.2:n.*575_*576del
NM_001320586.2:c.405-50344_405-50343del (ACYP2) NP_001307515.1:n.405-50344_405-50343del
NM_001320587.2:c.312-50344_312-50343del (ACYP2) NP_001307516.1:n.312-50344_312-50343del
NM_001320588.2:c.114-50344_114-50343del (ACYP2) NP_001307517.1:n.114-50344_114-50343del
NM_001320589.2:c.186-12952_186-12951del (ACYP2) NP_001307518.1:n.186-12952_186-12951del
NM_138448.4:c.186-50344_186-50343del (ACYP2) MANE Select NP_612457.1:n.186-50344_186-50343del