Canonical Allele Identifier: CA2789543026
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588099dup , CM000672.2:g.113588099dup GRCh38
NC_000010.10:g.115347858dup , CM000672.1:g.115347858dup GRCh37
NC_000010.9:g.115337848dup NCBI36
NG_008956.1:g.40081dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.1519-106dup MANE Select ENSP00000277903.4:n.1519-106dup
ENST00000351270.3:c.1519-106dup ENSP00000277903.4:n.1519-106dup
ENST00000542051.5:c.1441-106dup ENSP00000443283.1:n.1441-106dup
NM_001177660.1:c.1441-106dup NP_001171131.1:n.1441-106dup
NM_004132.3:c.1519-106dup NP_004123.1:n.1519-106dup
NM_001177660.2:c.1441-106dup NP_001171131.1:n.1441-106dup
NM_004132.4:c.1519-106dup NP_004123.1:n.1519-106dup
NM_004132.5:c.1519-106dup MANE Select NP_004123.1:n.1519-106dup
NM_001177660.3:c.1441-106dup NP_001171131.1:n.1441-106dup