Canonical Allele Identifier: CA1937429348
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1845721245

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588583_113588586dup , CM000672.2:g.113588583_113588586dup GRCh38
NC_000010.10:g.115348342_115348345dup , CM000672.1:g.115348342_115348345dup GRCh37
NC_000010.9:g.115338332_115338335dup NCBI36
NG_008956.1:g.40565_40568dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*214_*217dup MANE Select ENSP00000277903.4:n.*214_*217dup
ENST00000351270.3:c.*214_*217dup ENSP00000277903.4:n.*214_*217dup
ENST00000542051.5:c.*214_*217dup ENSP00000443283.1:n.*214_*217dup
NM_001177660.1:c.*214_*217dup NP_001171131.1:n.*214_*217dup
NM_004132.3:c.*214_*217dup NP_004123.1:n.*214_*217dup
NM_001177660.2:c.*214_*217dup NP_001171131.1:n.*214_*217dup
NM_004132.4:c.*214_*217dup NP_004123.1:n.*214_*217dup
NM_004132.5:c.*214_*217dup MANE Select NP_004123.1:n.*214_*217dup
NM_001177660.3:c.*214_*217dup NP_001171131.1:n.*214_*217dup