Canonical Allele Identifier: CA1937429190

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588310C= , CM000672.2:g.113588310C=	GRCh38
NC_000010.10:g.115348069C= , CM000672.1:g.115348069C=	GRCh37
NC_000010.9:g.115338059C=	NCBI36
NG_008956.1:g.40292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1624C= MANE Select	ENSP00000277903.4:p.Gln542=
ENST00000351270.3:c.1624C=	ENSP00000277903.4:p.Gln542=
ENST00000542051.5:c.1546C=	ENSP00000443283.1:p.Gln516=
NM_001177660.1:c.1546C=	NP_001171131.1:p.Gln516=
NM_004132.3:c.1624C=	NP_004123.1:p.Gln542=
NM_001177660.2:c.1546C=	NP_001171131.1:p.Gln516=
NM_004132.4:c.1624C=	NP_004123.1:p.Gln542=
NM_004132.5:c.1624C= MANE Select	NP_004123.1:p.Gln542=
NM_001177660.3:c.1546C=	NP_001171131.1:p.Gln516=