Canonical Allele Identifier: CA2544893047
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570899_113570900insGTGTAAGAAATGGGTC , CM000672.2:g.113570899_113570900insGTGTAAGAAATGGGTC GRCh38
NC_000010.10:g.115330658_115330659insGTGTAAGAAATGGGTC , CM000672.1:g.115330658_115330659insGTGTAAGAAATGGGTC GRCh37
NC_000010.9:g.115320648_115320649insGTGTAAGAAATGGGTC NCBI36
NG_008956.1:g.22881_22882insGTGTAAGAAATGGGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3374_106+3375insGTGTAAGAAATGGGTC MANE Select ENSP00000277903.4:n.106+3374_106+3375insGTGTAAGAAATGGGTC
ENST00000351270.3:c.106+3374_106+3375insGTGTAAGAAATGGGTC ENSP00000277903.4:n.106+3374_106+3375insGTGTAAGAAATGGGTC
ENST00000542051.5:c.28+3374_28+3375insGTGTAAGAAATGGGTC ENSP00000443283.1:n.28+3374_28+3375insGTGTAAGAAATGGGTC
NM_001177660.1:c.28+3374_28+3375insGTGTAAGAAATGGGTC NP_001171131.1:n.28+3374_28+3375insGTGTAAGAAATGGGTC
NM_004132.3:c.106+3374_106+3375insGTGTAAGAAATGGGTC NP_004123.1:n.106+3374_106+3375insGTGTAAGAAATGGGTC
NM_001177660.2:c.28+3374_28+3375insGTGTAAGAAATGGGTC NP_001171131.1:n.28+3374_28+3375insGTGTAAGAAATGGGTC
NM_004132.4:c.106+3374_106+3375insGTGTAAGAAATGGGTC NP_004123.1:n.106+3374_106+3375insGTGTAAGAAATGGGTC
NM_004132.5:c.106+3374_106+3375insGTGTAAGAAATGGGTC MANE Select NP_004123.1:n.106+3374_106+3375insGTGTAAGAAATGGGTC
NM_001177660.3:c.28+3374_28+3375insGTGTAAGAAATGGGTC NP_001171131.1:n.28+3374_28+3375insGTGTAAGAAATGGGTC