Canonical Allele Identifier: CA2652532217

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34268865_34268869del , CM000682.2:g.34268865_34268869del GRCh38
NC_000020.10:g.32856671_32856675del , CM000682.1:g.32856671_32856675del GRCh37
NC_000020.9:g.32320332_32320336del NCBI36
NG_011439.1:g.13501_13505del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374954.4:c.223-126_223-122del (ASIP) MANE Select ENSP00000364092.3:n.223-126_223-122del
ENST00000374954.3:c.223-126_223-122del (ASIP) ENSP00000364092.3:n.223-126_223-122del
ENST00000568305.5:c.223-126_223-122del (ASIP) ENSP00000454804.1:n.223-126_223-122del
NM_001672.2:c.223-126_223-122del (ASIP) NP_001663.2:n.223-126_223-122del
XM_005260412.2:c.235-126_235-122del (ASIP) XP_005260469.1:n.235-126_235-122del
XM_011528657.1:c.*7+12159_*7+12163del (AHCY) XP_011526959.1:n.*7+12159_*7+12163del
XM_011528820.1:c.223-126_223-122del (ASIP) XP_011527122.1:n.223-126_223-122del
XM_011528821.1:c.223-126_223-122del (ASIP) XP_011527123.1:n.223-126_223-122del
XM_011528822.1:c.223-126_223-122del (ASIP) XP_011527124.1:n.223-126_223-122del
XM_011528823.1:c.223-126_223-122del (ASIP) XP_011527125.1:n.223-126_223-122del
XM_005260412.3:c.235-126_235-122del (ASIP) XP_005260469.1:n.235-126_235-122del
XM_011528657.2:c.*7+12159_*7+12163del (AHCY) XP_011526959.2:n.*7+12159_*7+12163del
XM_011528820.2:c.223-126_223-122del (ASIP) XP_011527122.1:n.223-126_223-122del
NM_001385218.1:c.223-126_223-122del (ASIP) NP_001372147.1:n.223-126_223-122del
NM_001672.3:c.223-126_223-122del (ASIP) MANE Select NP_001663.2:n.223-126_223-122del