Canonical Allele Identifier: CA2789543029
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588486_113588495del , CM000672.2:g.113588486_113588495del GRCh38
NC_000010.10:g.115348245_115348254del , CM000672.1:g.115348245_115348254del GRCh37
NC_000010.9:g.115338235_115338244del NCBI36
NG_008956.1:g.40468_40477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*117_*126del MANE Select ENSP00000277903.4:n.*117_*126del
ENST00000351270.3:c.*117_*126del ENSP00000277903.4:n.*117_*126del
ENST00000542051.5:c.*117_*126del ENSP00000443283.1:n.*117_*126del
NM_001177660.1:c.*117_*126del NP_001171131.1:n.*117_*126del
NM_004132.3:c.*117_*126del NP_004123.1:n.*117_*126del
NM_001177660.2:c.*117_*126del NP_001171131.1:n.*117_*126del
NM_004132.4:c.*117_*126del NP_004123.1:n.*117_*126del
NM_004132.5:c.*117_*126del MANE Select NP_004123.1:n.*117_*126del
NM_001177660.3:c.*117_*126del NP_001171131.1:n.*117_*126del