Canonical Allele Identifier: CA1937429377
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588658_113588660delinsCAG , CM000672.2:g.113588658_113588660delinsCAG GRCh38
NC_000010.10:g.115348417_115348419delinsCAG , CM000672.1:g.115348417_115348419delinsCAG GRCh37
NC_000010.9:g.115338407_115338409delinsCAG NCBI36
NG_008956.1:g.40640_40642delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*289_*291delinsCAG MANE Select ENSP00000277903.4:n.*289_*291delinsCAG
ENST00000351270.3:c.*289_*291delinsCAG ENSP00000277903.4:n.*289_*291delinsCAG
ENST00000542051.5:c.*289_*291delinsCAG ENSP00000443283.1:n.*289_*291delinsCAG
NM_001177660.1:c.*289_*291delinsCAG NP_001171131.1:n.*289_*291delinsCAG
NM_004132.3:c.*289_*291delinsCAG NP_004123.1:n.*289_*291delinsCAG
NM_001177660.2:c.*289_*291delinsCAG NP_001171131.1:n.*289_*291delinsCAG
NM_004132.4:c.*289_*291delinsCAG NP_004123.1:n.*289_*291delinsCAG
NM_004132.5:c.*289_*291delinsCAG MANE Select NP_004123.1:n.*289_*291delinsCAG
NM_001177660.3:c.*289_*291delinsCAG NP_001171131.1:n.*289_*291delinsCAG