Canonical Allele Identifier: CA1937420411
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570895_113570899delinsAAACT , CM000672.2:g.113570895_113570899delinsAAACT GRCh38
NC_000010.10:g.115330654_115330658delinsAAACT , CM000672.1:g.115330654_115330658delinsAAACT GRCh37
NC_000010.9:g.115320644_115320648delinsAAACT NCBI36
NG_008956.1:g.22877_22881delinsAAACT

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3370_106+3374delinsAAACT MANE Select ENSP00000277903.4:n.106+3370_106+3374delinsAAACT
ENST00000351270.3:c.106+3370_106+3374delinsAAACT ENSP00000277903.4:n.106+3370_106+3374delinsAAACT
ENST00000542051.5:c.28+3370_28+3374delinsAAACT ENSP00000443283.1:n.28+3370_28+3374delinsAAACT
NM_001177660.1:c.28+3370_28+3374delinsAAACT NP_001171131.1:n.28+3370_28+3374delinsAAACT
NM_004132.3:c.106+3370_106+3374delinsAAACT NP_004123.1:n.106+3370_106+3374delinsAAACT
NM_001177660.2:c.28+3370_28+3374delinsAAACT NP_001171131.1:n.28+3370_28+3374delinsAAACT
NM_004132.4:c.106+3370_106+3374delinsAAACT NP_004123.1:n.106+3370_106+3374delinsAAACT
NM_004132.5:c.106+3370_106+3374delinsAAACT MANE Select NP_004123.1:n.106+3370_106+3374delinsAAACT
NM_001177660.3:c.28+3370_28+3374delinsAAACT NP_001171131.1:n.28+3370_28+3374delinsAAACT