Canonical Allele Identifier: CA2844241569

Gene: HABP2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588194_113588196dup , CM000672.2:g.113588194_113588196dup	GRCh38
NC_000010.10:g.115347953_115347955dup , CM000672.1:g.115347953_115347955dup	GRCh37
NC_000010.9:g.115337943_115337945dup	NCBI36
NG_008956.1:g.40176_40178dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.1519-11_1519-9dup MANE Select	ENSP00000277903.4:n.1519-11_1519-9dup
ENST00000351270.3:c.1519-11_1519-9dup	ENSP00000277903.4:n.1519-11_1519-9dup
ENST00000542051.5:c.1441-11_1441-9dup	ENSP00000443283.1:n.1441-11_1441-9dup
NM_001177660.1:c.1441-11_1441-9dup	NP_001171131.1:n.1441-11_1441-9dup
NM_004132.3:c.1519-11_1519-9dup	NP_004123.1:n.1519-11_1519-9dup
NM_001177660.2:c.1441-11_1441-9dup	NP_001171131.1:n.1441-11_1441-9dup
NM_004132.4:c.1519-11_1519-9dup	NP_004123.1:n.1519-11_1519-9dup
NM_004132.5:c.1519-11_1519-9dup MANE Select	NP_004123.1:n.1519-11_1519-9dup
NM_001177660.3:c.1441-11_1441-9dup	NP_001171131.1:n.1441-11_1441-9dup