Canonical Allele Identifier: CA2576219886
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248924_30248942del , CM000679.2:g.30248924_30248942del GRCh38
NC_000017.10:g.28575942_28575960del , CM000679.1:g.28575942_28575960del GRCh37
NC_000017.9:g.25600068_25600086del NCBI36
NG_011440.1:g.48115_48133del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*75_*93del MANE Select ENSP00000261714.6:n.*75_*93del
ENST00000261714.10:c.*75_*93del ENSP00000261714.6:n.*75_*93del
ENST00000578090.5:c.*1117_*1135del ENSP00000462353.1:n.*1117_*1135del
ENST00000578795.1:n.1342_1360del
NM_000386.3:c.*75_*93del NP_000377.1:n.*75_*93del
XR_934653.1:n.701-863_701-845del
XR_934655.1:n.701-3150_701-3132del
NM_000386.4:c.*75_*93del MANE Select NP_000377.1:n.*75_*93del