Canonical Allele Identifier: CA2610952677

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588646-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588647_113588648dup , CM000672.2:g.113588647_113588648dup	GRCh38
NC_000010.10:g.115348406_115348407dup , CM000672.1:g.115348406_115348407dup	GRCh37
NC_000010.9:g.115338396_115338397dup	NCBI36
NG_008956.1:g.40629_40630dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*278_*279dup MANE Select	ENSP00000277903.4:n.*278_*279dup
ENST00000351270.3:c.*278_*279dup	ENSP00000277903.4:n.*278_*279dup
ENST00000542051.5:c.*278_*279dup	ENSP00000443283.1:n.*278_*279dup
NM_001177660.1:c.*278_*279dup	NP_001171131.1:n.*278_*279dup
NM_004132.3:c.*278_*279dup	NP_004123.1:n.*278_*279dup
NM_001177660.2:c.*278_*279dup	NP_001171131.1:n.*278_*279dup
NM_004132.4:c.*278_*279dup	NP_004123.1:n.*278_*279dup
NM_004132.5:c.*278_*279dup MANE Select	NP_004123.1:n.*278_*279dup
NM_001177660.3:c.*278_*279dup	NP_001171131.1:n.*278_*279dup