Canonical Allele Identifier: CA2610952690

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588669-TCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588674_113588676del , CM000672.2:g.113588674_113588676del	GRCh38
NC_000010.10:g.115348433_115348435del , CM000672.1:g.115348433_115348435del	GRCh37
NC_000010.9:g.115338423_115338425del	NCBI36
NG_008956.1:g.40656_40658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*305_*307del MANE Select	ENSP00000277903.4:n.*305_*307del
ENST00000351270.3:c.*305_*307del	ENSP00000277903.4:n.*305_*307del
ENST00000542051.5:c.*305_*307del	ENSP00000443283.1:n.*305_*307del
NM_001177660.1:c.*305_*307del	NP_001171131.1:n.*305_*307del
NM_004132.3:c.*305_*307del	NP_004123.1:n.*305_*307del
NM_001177660.2:c.*305_*307del	NP_001171131.1:n.*305_*307del
NM_004132.4:c.*305_*307del	NP_004123.1:n.*305_*307del
NM_004132.5:c.*305_*307del MANE Select	NP_004123.1:n.*305_*307del
NM_001177660.3:c.*305_*307del	NP_001171131.1:n.*305_*307del