Canonical Allele Identifier: CA2610952638
Gene: HABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588596_113588618dup , CM000672.2:g.113588596_113588618dup GRCh38
NC_000010.10:g.115348355_115348377dup , CM000672.1:g.115348355_115348377dup GRCh37
NC_000010.9:g.115338345_115338367dup NCBI36
NG_008956.1:g.40578_40600dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*227_*249dup MANE Select ENSP00000277903.4:n.*227_*249dup
ENST00000351270.3:c.*227_*249dup ENSP00000277903.4:n.*227_*249dup
ENST00000542051.5:c.*227_*249dup ENSP00000443283.1:n.*227_*249dup
NM_001177660.1:c.*227_*249dup NP_001171131.1:n.*227_*249dup
NM_004132.3:c.*227_*249dup NP_004123.1:n.*227_*249dup
NM_001177660.2:c.*227_*249dup NP_001171131.1:n.*227_*249dup
NM_004132.4:c.*227_*249dup NP_004123.1:n.*227_*249dup
NM_004132.5:c.*227_*249dup MANE Select NP_004123.1:n.*227_*249dup
NM_001177660.3:c.*227_*249dup NP_001171131.1:n.*227_*249dup