Canonical Allele Identifier: CA2255117011
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30249008_30249009delinsAG , CM000679.2:g.30249008_30249009delinsAG GRCh38
NC_000017.10:g.28576026_28576027delinsAG , CM000679.1:g.28576026_28576027delinsAG GRCh37
NC_000017.9:g.25600152_25600153delinsAG NCBI36
NG_011440.1:g.48048_48049delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*8_*9delinsCT MANE Select ENSP00000261714.6:n.*8_*9delinsCT
ENST00000261714.10:c.*8_*9delinsCT ENSP00000261714.6:n.*8_*9delinsCT
ENST00000578090.5:c.*1050_*1051delinsCT ENSP00000462353.1:n.*1050_*1051delinsCT
ENST00000578795.1:n.1275_1276delinsCT
NM_000386.3:c.*8_*9delinsCT NP_000377.1:n.*8_*9delinsCT
XR_934653.1:n.701-779_701-778delinsAG
XR_934655.1:n.701-3066_701-3065delinsAG
NM_000386.4:c.*8_*9delinsCT MANE Select NP_000377.1:n.*8_*9delinsCT