Canonical Allele Identifier: CA2637004705
Gene: BLMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248895del , CM000679.2:g.30248895del GRCh38
NC_000017.10:g.28575913del , CM000679.1:g.28575913del GRCh37
NC_000017.9:g.25600039del NCBI36
NG_011440.1:g.48163del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*123del MANE Select ENSP00000261714.6:n.*123del
ENST00000261714.10:c.*123del ENSP00000261714.6:n.*123del
ENST00000578090.5:c.*1165del ENSP00000462353.1:n.*1165del
ENST00000578795.1:n.1390del
NM_000386.3:c.*123del NP_000377.1:n.*123del
XR_934653.1:n.701-892del
XR_934655.1:n.701-3179del
NM_000386.4:c.*123del MANE Select NP_000377.1:n.*123del