Canonical Allele Identifier: CA1937420339

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570766C= , CM000672.2:g.113570766C=	GRCh38
NC_000010.10:g.115330525C= , CM000672.1:g.115330525C=	GRCh37
NC_000010.9:g.115320515C=	NCBI36
NG_008956.1:g.22748C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.106+3241C= MANE Select	ENSP00000277903.4:n.106+3241C=
ENST00000351270.3:c.106+3241C=	ENSP00000277903.4:n.106+3241C=
ENST00000542051.5:c.28+3241C=	ENSP00000443283.1:n.28+3241C=
NM_001177660.1:c.28+3241C=	NP_001171131.1:n.28+3241C=
NM_004132.3:c.106+3241C=	NP_004123.1:n.106+3241C=
NM_001177660.2:c.28+3241C=	NP_001171131.1:n.28+3241C=
NM_004132.4:c.106+3241C=	NP_004123.1:n.106+3241C=
NM_004132.5:c.106+3241C= MANE Select	NP_004123.1:n.106+3241C=
NM_001177660.3:c.28+3241C=	NP_001171131.1:n.28+3241C=