Canonical Allele Identifier: CA2610952692
Gene: HABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588673_113588677del , CM000672.2:g.113588673_113588677del GRCh38
NC_000010.10:g.115348432_115348436del , CM000672.1:g.115348432_115348436del GRCh37
NC_000010.9:g.115338422_115338426del NCBI36
NG_008956.1:g.40655_40659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*304_*308del MANE Select ENSP00000277903.4:n.*304_*308del
ENST00000351270.3:c.*304_*308del ENSP00000277903.4:n.*304_*308del
ENST00000542051.5:c.*304_*308del ENSP00000443283.1:n.*304_*308del
NM_001177660.1:c.*304_*308del NP_001171131.1:n.*304_*308del
NM_004132.3:c.*304_*308del NP_004123.1:n.*304_*308del
NM_001177660.2:c.*304_*308del NP_001171131.1:n.*304_*308del
NM_004132.4:c.*304_*308del NP_004123.1:n.*304_*308del
NM_004132.5:c.*304_*308del MANE Select NP_004123.1:n.*304_*308del
NM_001177660.3:c.*304_*308del NP_001171131.1:n.*304_*308del