Canonical Allele Identifier: CA2652532203

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34268866_34268872del , CM000682.2:g.34268866_34268872del GRCh38
NC_000020.10:g.32856672_32856678del , CM000682.1:g.32856672_32856678del GRCh37
NC_000020.9:g.32320333_32320339del NCBI36
NG_011439.1:g.13502_13508del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374954.4:c.223-125_223-119del (ASIP) MANE Select ENSP00000364092.3:n.223-125_223-119del
ENST00000374954.3:c.223-125_223-119del (ASIP) ENSP00000364092.3:n.223-125_223-119del
ENST00000568305.5:c.223-125_223-119del (ASIP) ENSP00000454804.1:n.223-125_223-119del
NM_001672.2:c.223-125_223-119del (ASIP) NP_001663.2:n.223-125_223-119del
XM_005260412.2:c.235-125_235-119del (ASIP) XP_005260469.1:n.235-125_235-119del
XM_011528657.1:c.*7+12166_*7+12172del (AHCY) XP_011526959.1:n.*7+12166_*7+12172del
XM_011528820.1:c.223-125_223-119del (ASIP) XP_011527122.1:n.223-125_223-119del
XM_011528821.1:c.223-125_223-119del (ASIP) XP_011527123.1:n.223-125_223-119del
XM_011528822.1:c.223-125_223-119del (ASIP) XP_011527124.1:n.223-125_223-119del
XM_011528823.1:c.223-125_223-119del (ASIP) XP_011527125.1:n.223-125_223-119del
XM_005260412.3:c.235-125_235-119del (ASIP) XP_005260469.1:n.235-125_235-119del
XM_011528657.2:c.*7+12166_*7+12172del (AHCY) XP_011526959.2:n.*7+12166_*7+12172del
XM_011528820.2:c.223-125_223-119del (ASIP) XP_011527122.1:n.223-125_223-119del
NM_001385218.1:c.223-125_223-119del (ASIP) NP_001372147.1:n.223-125_223-119del
NM_001672.3:c.223-125_223-119del (ASIP) MANE Select NP_001663.2:n.223-125_223-119del