Canonical Allele Identifier: CA2574672137
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588438_113588440del , CM000672.2:g.113588438_113588440del GRCh38
NC_000010.10:g.115348197_115348199del , CM000672.1:g.115348197_115348199del GRCh37
NC_000010.9:g.115338187_115338189del NCBI36
NG_008956.1:g.40420_40422del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*69_*71del MANE Select ENSP00000277903.4:n.*69_*71del
ENST00000351270.3:c.*69_*71del ENSP00000277903.4:n.*69_*71del
ENST00000542051.5:c.*69_*71del ENSP00000443283.1:n.*69_*71del
NM_001177660.1:c.*69_*71del NP_001171131.1:n.*69_*71del
NM_004132.3:c.*69_*71del NP_004123.1:n.*69_*71del
NM_001177660.2:c.*69_*71del NP_001171131.1:n.*69_*71del
NM_004132.4:c.*69_*71del NP_004123.1:n.*69_*71del
NM_004132.5:c.*69_*71del MANE Select NP_004123.1:n.*69_*71del
NM_001177660.3:c.*69_*71del NP_001171131.1:n.*69_*71del