Canonical Allele Identifier: CA1937420425

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570920_113570922delinsCAA , CM000672.2:g.113570920_113570922delinsCAA	GRCh38
NC_000010.10:g.115330679_115330681delinsCAA , CM000672.1:g.115330679_115330681delinsCAA	GRCh37
NC_000010.9:g.115320669_115320671delinsCAA	NCBI36
NG_008956.1:g.22902_22904delinsCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.107-3369_107-3367delinsCAA MANE Select	ENSP00000277903.4:n.107-3369_107-3367delinsCAA
ENST00000351270.3:c.107-3369_107-3367delinsCAA	ENSP00000277903.4:n.107-3369_107-3367delinsCAA
ENST00000542051.5:c.29-3369_29-3367delinsCAA	ENSP00000443283.1:n.29-3369_29-3367delinsCAA
NM_001177660.1:c.29-3369_29-3367delinsCAA	NP_001171131.1:n.29-3369_29-3367delinsCAA
NM_004132.3:c.107-3369_107-3367delinsCAA	NP_004123.1:n.107-3369_107-3367delinsCAA
NM_001177660.2:c.29-3369_29-3367delinsCAA	NP_001171131.1:n.29-3369_29-3367delinsCAA
NM_004132.4:c.107-3369_107-3367delinsCAA	NP_004123.1:n.107-3369_107-3367delinsCAA
NM_004132.5:c.107-3369_107-3367delinsCAA MANE Select	NP_004123.1:n.107-3369_107-3367delinsCAA
NM_001177660.3:c.29-3369_29-3367delinsCAA	NP_001171131.1:n.29-3369_29-3367delinsCAA