Canonical Allele Identifier: CA2610952581
Gene: HABP2 HGNC NCBI

Linked Data

gnomAD v4: 10-113588520-GCCTT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588523_113588526del , CM000672.2:g.113588523_113588526del GRCh38
NC_000010.10:g.115348282_115348285del , CM000672.1:g.115348282_115348285del GRCh37
NC_000010.9:g.115338272_115338275del NCBI36
NG_008956.1:g.40505_40508del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*154_*157del MANE Select ENSP00000277903.4:n.*154_*157del
ENST00000351270.3:c.*154_*157del ENSP00000277903.4:n.*154_*157del
ENST00000542051.5:c.*154_*157del ENSP00000443283.1:n.*154_*157del
NM_001177660.1:c.*154_*157del NP_001171131.1:n.*154_*157del
NM_004132.3:c.*154_*157del NP_004123.1:n.*154_*157del
NM_001177660.2:c.*154_*157del NP_001171131.1:n.*154_*157del
NM_004132.4:c.*154_*157del NP_004123.1:n.*154_*157del
NM_004132.5:c.*154_*157del MANE Select NP_004123.1:n.*154_*157del
NM_001177660.3:c.*154_*157del NP_001171131.1:n.*154_*157del
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Search 100 bp 3'