Canonical Allele Identifier: CA393843139
Community Standard Title: NM_000057.4(BLM):c.1476C>A (p.Phe492Leu)
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90760849C>A , CM000677.2:g.90760849C>A GRCh38
NC_000015.9:g.91304079C>A , CM000677.1:g.91304079C>A GRCh37
NC_000015.8:g.89105083C>A NCBI36
NG_007272.1:g.48478C>A , LRG_20:g.48478C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000057.4:c.1476C>A MANE Select NP_000048.1:p.Phe492Leu
ENST00000355112.8:c.1476C>A MANE Select ENSP00000347232.3:p.Phe492Leu
NM_000057.3:c.1476C>A NP_000048.1:p.Phe492Leu
NM_001287246.1:c.1476C>A NP_001274175.1:p.Phe492Leu
NM_001287246.2:c.1476C>A NP_001274175.1:p.Phe492Leu
NM_001287247.1:c.1476C>A NP_001274176.1:p.Phe492Leu
NM_001287247.2:c.1476C>A NP_001274176.1:p.Phe492Leu
NM_001287248.1:c.351C>A NP_001274177.1:p.Phe117Leu
NM_001287248.2:c.351C>A NP_001274177.1:p.Phe117Leu
ENST00000355112.7:c.1476C>A ENSP00000347232.3:p.Phe492Leu
ENST00000559724.5:c.*400C>A ENSP00000453359.1:n.*400C>A
ENST00000560509.5:c.1476C>A ENSP00000454158.1:p.Phe492Leu
ENST00000648453.1:c.1476C>A ENSP00000497646.1:p.Phe492Leu
ENST00000680772.1:c.1476C>A ENSP00000506117.1:p.Phe492Leu
ENST00000681142.1:c.1476C>A ENSP00000506682.1:p.Phe492Leu
XM_011521881.1:c.162C>A XP_011520183.1:p.Phe54Leu
XM_011521881.2:c.162C>A XP_011520183.1:p.Phe54Leu
XM_011521882.1:c.1476C>A XP_011520184.1:p.Phe492Leu
XM_011521882.3:c.1476C>A XP_011520184.1:p.Phe492Leu