Canonical Allele Identifier: CA2610952606

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588544-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588547_113588548dup , CM000672.2:g.113588547_113588548dup	GRCh38
NC_000010.10:g.115348306_115348307dup , CM000672.1:g.115348306_115348307dup	GRCh37
NC_000010.9:g.115338296_115338297dup	NCBI36
NG_008956.1:g.40529_40530dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*178_*179dup MANE Select	ENSP00000277903.4:n.*178_*179dup
ENST00000351270.3:c.*178_*179dup	ENSP00000277903.4:n.*178_*179dup
ENST00000542051.5:c.*178_*179dup	ENSP00000443283.1:n.*178_*179dup
NM_001177660.1:c.*178_*179dup	NP_001171131.1:n.*178_*179dup
NM_004132.3:c.*178_*179dup	NP_004123.1:n.*178_*179dup
NM_001177660.2:c.*178_*179dup	NP_001171131.1:n.*178_*179dup
NM_004132.4:c.*178_*179dup	NP_004123.1:n.*178_*179dup
NM_004132.5:c.*178_*179dup MANE Select	NP_004123.1:n.*178_*179dup
NM_001177660.3:c.*178_*179dup	NP_001171131.1:n.*178_*179dup