Canonical Allele Identifier: CA2574672130
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588401_113588402del , CM000672.2:g.113588401_113588402del GRCh38
NC_000010.10:g.115348160_115348161del , CM000672.1:g.115348160_115348161del GRCh37
NC_000010.9:g.115338150_115338151del NCBI36
NG_008956.1:g.40383_40384del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*32_*33del MANE Select ENSP00000277903.4:n.*32_*33del
ENST00000351270.3:c.*32_*33del ENSP00000277903.4:n.*32_*33del
ENST00000542051.5:c.*32_*33del ENSP00000443283.1:n.*32_*33del
NM_001177660.1:c.*32_*33del NP_001171131.1:n.*32_*33del
NM_004132.3:c.*32_*33del NP_004123.1:n.*32_*33del
NM_001177660.2:c.*32_*33del NP_001171131.1:n.*32_*33del
NM_004132.4:c.*32_*33del NP_004123.1:n.*32_*33del
NM_004132.5:c.*32_*33del MANE Select NP_004123.1:n.*32_*33del
NM_001177660.3:c.*32_*33del NP_001171131.1:n.*32_*33del