Canonical Allele Identifier: CA660073181

Gene: HABP2

Linked Data

• dbSNP Id: rs1554848409
• MyVariant Identifiers: chr10:g.115348363_115348364insATAGT (hg19) ; chr10:g.113588604_113588605insATAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113588607_113588611dup , CM000672.2:g.113588607_113588611dup	GRCh38
NC_000010.10:g.115348366_115348370dup , CM000672.1:g.115348366_115348370dup	GRCh37
NC_000010.9:g.115338356_115338360dup	NCBI36
NG_008956.1:g.40589_40593dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.*238_*242dup MANE Select	ENSP00000277903.4:n.*238_*242dup
ENST00000351270.3:c.*238_*242dup	ENSP00000277903.4:n.*238_*242dup
ENST00000542051.5:c.*238_*242dup	ENSP00000443283.1:n.*238_*242dup
NM_001177660.1:c.*238_*242dup	NP_001171131.1:n.*238_*242dup
NM_004132.3:c.*238_*242dup	NP_004123.1:n.*238_*242dup
NM_001177660.2:c.*238_*242dup	NP_001171131.1:n.*238_*242dup
NM_004132.4:c.*238_*242dup	NP_004123.1:n.*238_*242dup
NM_004132.5:c.*238_*242dup MANE Select	NP_004123.1:n.*238_*242dup
NM_001177660.3:c.*238_*242dup	NP_001171131.1:n.*238_*242dup