Canonical Allele Identifier: CA2637004724
Gene: BLMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248916dup , CM000679.2:g.30248916dup GRCh38
NC_000017.10:g.28575934dup , CM000679.1:g.28575934dup GRCh37
NC_000017.9:g.25600060dup NCBI36
NG_011440.1:g.48142dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*102dup MANE Select ENSP00000261714.6:n.*102dup
ENST00000261714.10:c.*102dup ENSP00000261714.6:n.*102dup
ENST00000578090.5:c.*1144dup ENSP00000462353.1:n.*1144dup
ENST00000578795.1:n.1369dup
NM_000386.3:c.*102dup NP_000377.1:n.*102dup
XR_934653.1:n.701-871dup
XR_934655.1:n.701-3158dup
NM_000386.4:c.*102dup MANE Select NP_000377.1:n.*102dup