Canonical Allele Identifier: CA1937429379

Gene: HABP2

Linked Data

• dbSNP Id: rs1845725387

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588660_113588663dup , CM000672.2:g.113588660_113588663dup	GRCh38
NC_000010.10:g.115348419_115348422dup , CM000672.1:g.115348419_115348422dup	GRCh37
NC_000010.9:g.115338409_115338412dup	NCBI36
NG_008956.1:g.40642_40645dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*291_*294dup MANE Select	ENSP00000277903.4:n.*291_*294dup
ENST00000351270.3:c.*291_*294dup	ENSP00000277903.4:n.*291_*294dup
ENST00000542051.5:c.*291_*294dup	ENSP00000443283.1:n.*291_*294dup
NM_001177660.1:c.*291_*294dup	NP_001171131.1:n.*291_*294dup
NM_004132.3:c.*291_*294dup	NP_004123.1:n.*291_*294dup
NM_001177660.2:c.*291_*294dup	NP_001171131.1:n.*291_*294dup
NM_004132.4:c.*291_*294dup	NP_004123.1:n.*291_*294dup
NM_004132.5:c.*291_*294dup MANE Select	NP_004123.1:n.*291_*294dup
NM_001177660.3:c.*291_*294dup	NP_001171131.1:n.*291_*294dup