Canonical Allele Identifier: CA1937429378

Gene: HABP2

Linked Data

• dbSNP Id: rs1845725387
• gnomAD v4: 10-113588658-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588662_113588663del , CM000672.2:g.113588662_113588663del	GRCh38
NC_000010.10:g.115348421_115348422del , CM000672.1:g.115348421_115348422del	GRCh37
NC_000010.9:g.115338411_115338412del	NCBI36
NG_008956.1:g.40644_40645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*293_*294del MANE Select	ENSP00000277903.4:n.*293_*294del
ENST00000351270.3:c.*293_*294del	ENSP00000277903.4:n.*293_*294del
ENST00000542051.5:c.*293_*294del	ENSP00000443283.1:n.*293_*294del
NM_001177660.1:c.*293_*294del	NP_001171131.1:n.*293_*294del
NM_004132.3:c.*293_*294del	NP_004123.1:n.*293_*294del
NM_001177660.2:c.*293_*294del	NP_001171131.1:n.*293_*294del
NM_004132.4:c.*293_*294del	NP_004123.1:n.*293_*294del
NM_004132.5:c.*293_*294del MANE Select	NP_004123.1:n.*293_*294del
NM_001177660.3:c.*293_*294del	NP_001171131.1:n.*293_*294del