Canonical Allele Identifier: CA274770264

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90798216C>T , CM000677.2:g.90798216C>T	GRCh38
NC_000015.9:g.91341446C>T , CM000677.1:g.91341446C>T	GRCh37
NC_000015.8:g.89142450C>T	NCBI36
NG_007272.1:g.85845C>T , LRG_20:g.85845C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000057.4:c.3237C>T MANE Select	NP_000048.1:p.Asp1079=
ENST00000355112.8:c.3237C>T MANE Select	ENSP00000347232.3:p.Asp1079=
NM_000057.3:c.3237C>T	NP_000048.1:p.Asp1079=
NM_001287246.1:c.3237C>T	NP_001274175.1:p.Asp1079=
NM_001287246.2:c.3237C>T	NP_001274175.1:p.Asp1079=
NM_001287247.1:c.3237C>T	NP_001274176.1:p.Asp1079=
NM_001287247.2:c.3237C>T	NP_001274176.1:p.Asp1079=
NM_001287248.1:c.2112C>T	NP_001274177.1:p.Asp704=
NM_001287248.2:c.2112C>T	NP_001274177.1:p.Asp704=
ENST00000355112.7:c.3237C>T	ENSP00000347232.3:p.Asp1079=
ENST00000558825.5:n.584C>T
ENST00000559724.5:c.*2161C>T	ENSP00000453359.1:n.*2161C>T
ENST00000560136.5:n.1263C>T
ENST00000560509.5:c.3237C>T	ENSP00000454158.1:p.Asp1079=
ENST00000560559.2:n.1810C>T
ENST00000648453.1:c.3237C>T	ENSP00000497646.1:p.Asp1079=
ENST00000680772.1:c.3237C>T	ENSP00000506117.1:p.Asp1079=
ENST00000681142.1:c.3237C>T	ENSP00000506682.1:p.Asp1079=
XM_006720632.2:c.1275C>T	XP_006720695.1:p.Asp425=
XM_011521881.1:c.1923C>T	XP_011520183.1:p.Asp641=
XM_011521881.2:c.1923C>T	XP_011520183.1:p.Asp641=