Canonical Allele Identifier: CA1937419470

Gene: HABP2

Linked Data

• dbSNP Id: rs1845255998

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113569136del , CM000672.2:g.113569136del	GRCh38
NC_000010.10:g.115328895del , CM000672.1:g.115328895del	GRCh37
NC_000010.9:g.115318885del	NCBI36
NG_008956.1:g.21118del

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.106+1611del MANE Select	ENSP00000277903.4:n.106+1611del
ENST00000351270.3:c.106+1611del	ENSP00000277903.4:n.106+1611del
ENST00000460714.1:n.43-508del
ENST00000542051.5:c.28+1611del	ENSP00000443283.1:n.28+1611del
NM_001177660.1:c.28+1611del	NP_001171131.1:n.28+1611del
NM_004132.3:c.106+1611del	NP_004123.1:n.106+1611del
NM_001177660.2:c.28+1611del	NP_001171131.1:n.28+1611del
NM_004132.4:c.106+1611del	NP_004123.1:n.106+1611del
NM_004132.5:c.106+1611del MANE Select	NP_004123.1:n.106+1611del
NM_001177660.3:c.28+1611del	NP_001171131.1:n.28+1611del