Canonical Allele Identifier: CA2195302335

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811235C= , CM000677.2:g.90811235C=	GRCh38
NC_000015.9:g.91354465C= , CM000677.1:g.91354465C=	GRCh37
NC_000015.8:g.89155469C=	NCBI36
NG_007272.1:g.98864C= , LRG_20:g.98864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3905C= MANE Select	ENSP00000347232.3:p.Ser1302=
ENST00000560559.2:n.2478C=
ENST00000648453.1:c.3905C=	ENSP00000497646.1:p.Ser1302=
ENST00000680772.1:c.3905C=	ENSP00000506117.1:p.Ser1302=
ENST00000681142.1:c.3905C=	ENSP00000506682.1:p.Ser1302=
ENST00000355112.7:c.3905C=	ENSP00000347232.3:p.Ser1302=
ENST00000558825.5:n.1252C=
ENST00000559724.5:c.*2829C=	ENSP00000453359.1:n.*2829C=
ENST00000560136.5:n.1931C=
ENST00000560509.5:c.3512C=	ENSP00000454158.1:p.Ser1171=
ENST00000560821.1:n.325C=
NM_000057.3:c.3905C=	NP_000048.1:p.Ser1302=
NM_001287246.1:c.3905C=	NP_001274175.1:p.Ser1302=
NM_001287247.1:c.3512C=	NP_001274176.1:p.Ser1171=
NM_001287248.1:c.2780C=	NP_001274177.1:p.Ser927=
XM_006720632.2:c.1943C=	XP_006720695.1:p.Ser648=
XM_011521881.1:c.2591C=	XP_011520183.1:p.Ser864=
XM_011521881.2:c.2591C=	XP_011520183.1:p.Ser864=
NM_000057.4:c.3905C= MANE Select	NP_000048.1:p.Ser1302=
NM_001287246.2:c.3905C=	NP_001274175.1:p.Ser1302=
NM_001287247.2:c.3512C=	NP_001274176.1:p.Ser1171=
NM_001287248.2:c.2780C=	NP_001274177.1:p.Ser927=