Canonical Allele Identifier: CA932715898

Gene: HABP2

Linked Data

• dbSNP Id: rs1845721864
• gnomAD v3: 10-113588595-T-TCAA
• gnomAD v4: 10-113588595-T-TCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588598_113588600dup , CM000672.2:g.113588598_113588600dup	GRCh38
NC_000010.10:g.115348357_115348359dup , CM000672.1:g.115348357_115348359dup	GRCh37
NC_000010.9:g.115338347_115338349dup	NCBI36
NG_008956.1:g.40580_40582dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*229_*231dup MANE Select	ENSP00000277903.4:n.*229_*231dup
ENST00000351270.3:c.*229_*231dup	ENSP00000277903.4:n.*229_*231dup
ENST00000542051.5:c.*229_*231dup	ENSP00000443283.1:n.*229_*231dup
NM_001177660.1:c.*229_*231dup	NP_001171131.1:n.*229_*231dup
NM_004132.3:c.*229_*231dup	NP_004123.1:n.*229_*231dup
NM_001177660.2:c.*229_*231dup	NP_001171131.1:n.*229_*231dup
NM_004132.4:c.*229_*231dup	NP_004123.1:n.*229_*231dup
NM_004132.5:c.*229_*231dup MANE Select	NP_004123.1:n.*229_*231dup
NM_001177660.3:c.*229_*231dup	NP_001171131.1:n.*229_*231dup