Canonical Allele Identifier: CA2580953912

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570889T>G , CM000672.2:g.113570889T>G	GRCh38
NC_000010.10:g.115330648T>G , CM000672.1:g.115330648T>G	GRCh37
NC_000010.9:g.115320638T>G	NCBI36
NG_008956.1:g.22871T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.106+3364T>G MANE Select	ENSP00000277903.4:n.106+3364T>G
ENST00000351270.3:c.106+3364T>G	ENSP00000277903.4:n.106+3364T>G
ENST00000542051.5:c.28+3364T>G	ENSP00000443283.1:n.28+3364T>G
NM_001177660.1:c.28+3364T>G	NP_001171131.1:n.28+3364T>G
NM_004132.3:c.106+3364T>G	NP_004123.1:n.106+3364T>G
NM_001177660.2:c.28+3364T>G	NP_001171131.1:n.28+3364T>G
NM_004132.4:c.106+3364T>G	NP_004123.1:n.106+3364T>G
NM_004132.5:c.106+3364T>G MANE Select	NP_004123.1:n.106+3364T>G
NM_001177660.3:c.28+3364T>G	NP_001171131.1:n.28+3364T>G