Canonical Allele Identifier: CA1937429265

Gene: HABP2

Linked Data

• dbSNP Id: rs1845712111
• gnomAD v4: 10-113588434-C-CCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588438_113588440dup , CM000672.2:g.113588438_113588440dup	GRCh38
NC_000010.10:g.115348197_115348199dup , CM000672.1:g.115348197_115348199dup	GRCh37
NC_000010.9:g.115338187_115338189dup	NCBI36
NG_008956.1:g.40420_40422dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*69_*71dup MANE Select	ENSP00000277903.4:n.*69_*71dup
ENST00000351270.3:c.*69_*71dup	ENSP00000277903.4:n.*69_*71dup
ENST00000542051.5:c.*69_*71dup	ENSP00000443283.1:n.*69_*71dup
NM_001177660.1:c.*69_*71dup	NP_001171131.1:n.*69_*71dup
NM_004132.3:c.*69_*71dup	NP_004123.1:n.*69_*71dup
NM_001177660.2:c.*69_*71dup	NP_001171131.1:n.*69_*71dup
NM_004132.4:c.*69_*71dup	NP_004123.1:n.*69_*71dup
NM_004132.5:c.*69_*71dup MANE Select	NP_004123.1:n.*69_*71dup
NM_001177660.3:c.*69_*71dup	NP_001171131.1:n.*69_*71dup