Canonical Allele Identifier: CA1937429368

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588627C= , CM000672.2:g.113588627C=	GRCh38
NC_000010.10:g.115348386C= , CM000672.1:g.115348386C=	GRCh37
NC_000010.9:g.115338376C=	NCBI36
NG_008956.1:g.40609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*258C= MANE Select	ENSP00000277903.4:n.*258C=
ENST00000351270.3:c.*258C=	ENSP00000277903.4:n.*258C=
ENST00000542051.5:c.*258C=	ENSP00000443283.1:n.*258C=
NM_001177660.1:c.*258C=	NP_001171131.1:n.*258C=
NM_004132.3:c.*258C=	NP_004123.1:n.*258C=
NM_001177660.2:c.*258C=	NP_001171131.1:n.*258C=
NM_004132.4:c.*258C=	NP_004123.1:n.*258C=
NM_004132.5:c.*258C= MANE Select	NP_004123.1:n.*258C=
NM_001177660.3:c.*258C=	NP_001171131.1:n.*258C=