Canonical Allele Identifier: CA2569895852

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571303T>C , CM000672.2:g.113571303T>C	GRCh38
NC_000010.10:g.115331062T>C , CM000672.1:g.115331062T>C	GRCh37
NC_000010.9:g.115321052T>C	NCBI36
NG_008956.1:g.23285T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-2986T>C MANE Select	ENSP00000277903.4:n.107-2986T>C
ENST00000351270.3:c.107-2986T>C	ENSP00000277903.4:n.107-2986T>C
ENST00000542051.5:c.29-2986T>C	ENSP00000443283.1:n.29-2986T>C
NM_001177660.1:c.29-2986T>C	NP_001171131.1:n.29-2986T>C
NM_004132.3:c.107-2986T>C	NP_004123.1:n.107-2986T>C
NM_001177660.2:c.29-2986T>C	NP_001171131.1:n.29-2986T>C
NM_004132.4:c.107-2986T>C	NP_004123.1:n.107-2986T>C
NM_004132.5:c.107-2986T>C MANE Select	NP_004123.1:n.107-2986T>C
NM_001177660.3:c.29-2986T>C	NP_001171131.1:n.29-2986T>C