Canonical Allele Identifier: CA1937419469

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113569134_113569135delinsAG , CM000672.2:g.113569134_113569135delinsAG	GRCh38
NC_000010.10:g.115328893_115328894delinsAG , CM000672.1:g.115328893_115328894delinsAG	GRCh37
NC_000010.9:g.115318883_115318884delinsAG	NCBI36
NG_008956.1:g.21116_21117delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.106+1609_106+1610delinsAG MANE Select	ENSP00000277903.4:n.106+1609_106+1610delinsAG
ENST00000351270.3:c.106+1609_106+1610delinsAG	ENSP00000277903.4:n.106+1609_106+1610delinsAG
ENST00000460714.1:n.43-510_43-509delinsAG
ENST00000542051.5:c.28+1609_28+1610delinsAG	ENSP00000443283.1:n.28+1609_28+1610delinsAG
NM_001177660.1:c.28+1609_28+1610delinsAG	NP_001171131.1:n.28+1609_28+1610delinsAG
NM_004132.3:c.106+1609_106+1610delinsAG	NP_004123.1:n.106+1609_106+1610delinsAG
NM_001177660.2:c.28+1609_28+1610delinsAG	NP_001171131.1:n.28+1609_28+1610delinsAG
NM_004132.4:c.106+1609_106+1610delinsAG	NP_004123.1:n.106+1609_106+1610delinsAG
NM_004132.5:c.106+1609_106+1610delinsAG MANE Select	NP_004123.1:n.106+1609_106+1610delinsAG
NM_001177660.3:c.28+1609_28+1610delinsAG	NP_001171131.1:n.28+1609_28+1610delinsAG