Canonical Allele Identifier: CA2610952392

Gene: HABP2

Linked Data

• gnomAD v4: 10-113588128-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588133del , CM000672.2:g.113588133del	GRCh38
NC_000010.10:g.115347892del , CM000672.1:g.115347892del	GRCh37
NC_000010.9:g.115337882del	NCBI36
NG_008956.1:g.40115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-72del MANE Select	ENSP00000277903.4:n.1519-72del
ENST00000351270.3:c.1519-72del	ENSP00000277903.4:n.1519-72del
ENST00000542051.5:c.1441-72del	ENSP00000443283.1:n.1441-72del
NM_001177660.1:c.1441-72del	NP_001171131.1:n.1441-72del
NM_004132.3:c.1519-72del	NP_004123.1:n.1519-72del
NM_001177660.2:c.1441-72del	NP_001171131.1:n.1441-72del
NM_004132.4:c.1519-72del	NP_004123.1:n.1519-72del
NM_004132.5:c.1519-72del MANE Select	NP_004123.1:n.1519-72del
NM_001177660.3:c.1441-72del	NP_001171131.1:n.1441-72del