Canonical Allele Identifier: CA2255117040
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30249072T= , CM000679.2:g.30249072T= GRCh38
NC_000017.10:g.28576090T= , CM000679.1:g.28576090T= GRCh37
NC_000017.9:g.25600216T= NCBI36
NG_011440.1:g.47985A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.1313A= MANE Select ENSP00000261714.6:p.Glu438=
ENST00000261714.10:c.1313A= ENSP00000261714.6:p.Glu438=
ENST00000578090.5:c.*987A= ENSP00000462353.1:n.*987A=
ENST00000578795.1:n.1212A=
NM_000386.3:c.1313A= NP_000377.1:p.Glu438=
XR_934653.1:n.701-715T=
XR_934655.1:n.701-3002T=
NM_000386.4:c.1313A= MANE Select NP_000377.1:p.Glu438=