Canonical Allele Identifier: CA393848033

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90804236C>T , CM000677.2:g.90804236C>T	GRCh38
NC_000015.9:g.91347466C>T , CM000677.1:g.91347466C>T	GRCh37
NC_000015.8:g.89148470C>T	NCBI36
NG_007272.1:g.91865C>T , LRG_20:g.91865C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000057.4:c.3628C>T MANE Select	NP_000048.1:p.Gln1210Ter
ENST00000355112.8:c.3628C>T MANE Select	ENSP00000347232.3:p.Gln1210Ter
NM_000057.3:c.3628C>T	NP_000048.1:p.Gln1210Ter
NM_001287246.1:c.3628C>T	NP_001274175.1:p.Gln1210Ter
NM_001287246.2:c.3628C>T	NP_001274175.1:p.Gln1210Ter
NM_001287247.1:c.3359-4901C>T	NP_001274176.1:n.3359-4901C>T
NM_001287247.2:c.3359-4901C>T	NP_001274176.1:n.3359-4901C>T
NM_001287248.1:c.2503C>T	NP_001274177.1:p.Gln835Ter
NM_001287248.2:c.2503C>T	NP_001274177.1:p.Gln835Ter
ENST00000355112.7:c.3628C>T	ENSP00000347232.3:p.Gln1210Ter
ENST00000558825.5:n.975C>T
ENST00000559724.5:c.*2552C>T	ENSP00000453359.1:n.*2552C>T
ENST00000560136.5:n.1654C>T
ENST00000560509.5:c.3359-4901C>T	ENSP00000454158.1:n.3359-4901C>T
ENST00000560559.2:n.2201C>T
ENST00000648453.1:c.3628C>T	ENSP00000497646.1:p.Gln1210Ter
ENST00000680772.1:c.3628C>T	ENSP00000506117.1:p.Gln1210Ter
ENST00000681142.1:c.3628C>T	ENSP00000506682.1:p.Gln1210Ter
XM_006720632.2:c.1666C>T	XP_006720695.1:p.Gln556Ter
XM_011521881.1:c.2314C>T	XP_011520183.1:p.Gln772Ter
XM_011521881.2:c.2314C>T	XP_011520183.1:p.Gln772Ter