Canonical Allele Identifier: CA2195297301

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90794227T= , CM000677.2:g.90794227T=	GRCh38
NC_000015.9:g.91337457T= , CM000677.1:g.91337457T=	GRCh37
NC_000015.8:g.89138461T=	NCBI36
NG_007272.1:g.81856T= , LRG_20:g.81856T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3080T= MANE Select	ENSP00000347232.3:p.Val1027=
ENST00000560559.2:n.1653T=
ENST00000648453.1:c.3080T=	ENSP00000497646.1:p.Val1027=
ENST00000680772.1:c.3080T=	ENSP00000506117.1:p.Val1027=
ENST00000681142.1:c.3080T=	ENSP00000506682.1:p.Val1027=
ENST00000355112.7:c.3080T=	ENSP00000347232.3:p.Val1027=
ENST00000558825.5:n.427T=
ENST00000559724.5:c.*2004T=	ENSP00000453359.1:n.*2004T=
ENST00000560136.5:n.1106T=
ENST00000560509.5:c.3080T=	ENSP00000454158.1:p.Val1027=
ENST00000560559.1:n.617T=
NM_000057.3:c.3080T=	NP_000048.1:p.Val1027=
NM_001287246.1:c.3080T=	NP_001274175.1:p.Val1027=
NM_001287247.1:c.3080T=	NP_001274176.1:p.Val1027=
NM_001287248.1:c.1955T=	NP_001274177.1:p.Val652=
XM_006720632.2:c.1118T=	XP_006720695.1:p.Val373=
XM_011521881.1:c.1766T=	XP_011520183.1:p.Val589=
XM_011521881.2:c.1766T=	XP_011520183.1:p.Val589=
NM_000057.4:c.3080T= MANE Select	NP_000048.1:p.Val1027=
NM_001287246.2:c.3080T=	NP_001274175.1:p.Val1027=
NM_001287247.2:c.3080T=	NP_001274176.1:p.Val1027=
NM_001287248.2:c.1955T=	NP_001274177.1:p.Val652=