Canonical Allele Identifier: CA1937429105

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588166T= , CM000672.2:g.113588166T=	GRCh38
NC_000010.10:g.115347925T= , CM000672.1:g.115347925T=	GRCh37
NC_000010.9:g.115337915T=	NCBI36
NG_008956.1:g.40148T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-39T= MANE Select	ENSP00000277903.4:n.1519-39T=
ENST00000351270.3:c.1519-39T=	ENSP00000277903.4:n.1519-39T=
ENST00000542051.5:c.1441-39T=	ENSP00000443283.1:n.1441-39T=
NM_001177660.1:c.1441-39T=	NP_001171131.1:n.1441-39T=
NM_004132.3:c.1519-39T=	NP_004123.1:n.1519-39T=
NM_001177660.2:c.1441-39T=	NP_001171131.1:n.1441-39T=
NM_004132.4:c.1519-39T=	NP_004123.1:n.1519-39T=
NM_004132.5:c.1519-39T= MANE Select	NP_004123.1:n.1519-39T=
NM_001177660.3:c.1441-39T=	NP_001171131.1:n.1441-39T=