Canonical Allele Identifier: CA2195295790

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90790764C= , CM000677.2:g.90790764C=	GRCh38
NC_000015.9:g.91333994C= , CM000677.1:g.91333994C=	GRCh37
NC_000015.8:g.89134998C=	NCBI36
NG_007272.1:g.78393C= , LRG_20:g.78393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.2939C= MANE Select	ENSP00000347232.3:p.Ala980=
ENST00000560559.2:n.1512C=
ENST00000648453.1:c.2939C=	ENSP00000497646.1:p.Ala980=
ENST00000680772.1:c.2939C=	ENSP00000506117.1:p.Ala980=
ENST00000681142.1:c.2939C=	ENSP00000506682.1:p.Ala980=
ENST00000355112.7:c.2939C=	ENSP00000347232.3:p.Ala980=
ENST00000559724.5:c.*1863C=	ENSP00000453359.1:n.*1863C=
ENST00000560136.5:n.965C=
ENST00000560509.5:c.2939C=	ENSP00000454158.1:p.Ala980=
ENST00000560559.1:n.476C=
NM_000057.3:c.2939C=	NP_000048.1:p.Ala980=
NM_001287246.1:c.2939C=	NP_001274175.1:p.Ala980=
NM_001287247.1:c.2939C=	NP_001274176.1:p.Ala980=
NM_001287248.1:c.1814C=	NP_001274177.1:p.Ala605=
XM_006720632.2:c.977C=	XP_006720695.1:p.Ala326=
XM_011521881.1:c.1625C=	XP_011520183.1:p.Ala542=
XM_011521881.2:c.1625C=	XP_011520183.1:p.Ala542=
NM_000057.4:c.2939C= MANE Select	NP_000048.1:p.Ala980=
NM_001287246.2:c.2939C=	NP_001274175.1:p.Ala980=
NM_001287247.2:c.2939C=	NP_001274176.1:p.Ala980=
NM_001287248.2:c.1814C=	NP_001274177.1:p.Ala605=