Canonical Allele Identifier: CA2610952318

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588060-G-GCCTTGTCACTGCTTTCCAGAGAAGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588062_113588087dup , CM000672.2:g.113588062_113588087dup	GRCh38
NC_000010.10:g.115347821_115347846dup , CM000672.1:g.115347821_115347846dup	GRCh37
NC_000010.9:g.115337811_115337836dup	NCBI36
NG_008956.1:g.40044_40069dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-143_1519-118dup MANE Select	ENSP00000277903.4:n.1519-143_1519-118dup
ENST00000351270.3:c.1519-143_1519-118dup	ENSP00000277903.4:n.1519-143_1519-118dup
ENST00000542051.5:c.1441-143_1441-118dup	ENSP00000443283.1:n.1441-143_1441-118dup
NM_001177660.1:c.1441-143_1441-118dup	NP_001171131.1:n.1441-143_1441-118dup
NM_004132.3:c.1519-143_1519-118dup	NP_004123.1:n.1519-143_1519-118dup
NM_001177660.2:c.1441-143_1441-118dup	NP_001171131.1:n.1441-143_1441-118dup
NM_004132.4:c.1519-143_1519-118dup	NP_004123.1:n.1519-143_1519-118dup
NM_004132.5:c.1519-143_1519-118dup MANE Select	NP_004123.1:n.1519-143_1519-118dup
NM_001177660.3:c.1441-143_1441-118dup	NP_001171131.1:n.1441-143_1441-118dup