Canonical Allele Identifier: CA2789543030
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588510_113588511insT , CM000672.2:g.113588510_113588511insT GRCh38
NC_000010.10:g.115348269_115348270insT , CM000672.1:g.115348269_115348270insT GRCh37
NC_000010.9:g.115338259_115338260insT NCBI36
NG_008956.1:g.40492_40493insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*141_*142insT MANE Select ENSP00000277903.4:n.*141_*142insT
ENST00000351270.3:c.*141_*142insT ENSP00000277903.4:n.*141_*142insT
ENST00000542051.5:c.*141_*142insT ENSP00000443283.1:n.*141_*142insT
NM_001177660.1:c.*141_*142insT NP_001171131.1:n.*141_*142insT
NM_004132.3:c.*141_*142insT NP_004123.1:n.*141_*142insT
NM_001177660.2:c.*141_*142insT NP_001171131.1:n.*141_*142insT
NM_004132.4:c.*141_*142insT NP_004123.1:n.*141_*142insT
NM_004132.5:c.*141_*142insT MANE Select NP_004123.1:n.*141_*142insT
NM_001177660.3:c.*141_*142insT NP_001171131.1:n.*141_*142insT