Canonical Allele Identifier: CA1937429177

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588287G= , CM000672.2:g.113588287G=	GRCh38
NC_000010.10:g.115348046G= , CM000672.1:g.115348046G=	GRCh37
NC_000010.9:g.115338036G=	NCBI36
NG_008956.1:g.40269G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.1601G= MANE Select	ENSP00000277903.4:p.Gly534=
ENST00000351270.3:c.1601G=	ENSP00000277903.4:p.Gly534=
ENST00000542051.5:c.1523G=	ENSP00000443283.1:p.Gly508=
NM_001177660.1:c.1523G=	NP_001171131.1:p.Gly508=
NM_004132.3:c.1601G=	NP_004123.1:p.Gly534=
NM_001177660.2:c.1523G=	NP_001171131.1:p.Gly508=
NM_004132.4:c.1601G=	NP_004123.1:p.Gly534=
NM_004132.5:c.1601G= MANE Select	NP_004123.1:p.Gly534=
NM_001177660.3:c.1523G=	NP_001171131.1:p.Gly508=