Canonical Allele Identifier: CA393847872

Gene: BLM

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90804166G>A , CM000677.2:g.90804166G>A	GRCh38
NC_000015.9:g.91347396G>A , CM000677.1:g.91347396G>A	GRCh37
NC_000015.8:g.89148400G>A	NCBI36
NG_007272.1:g.91795G>A , LRG_20:g.91795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3559-1G>A MANE Select	ENSP00000347232.3:n.3559-1G>A
ENST00000560559.2:n.2132-1G>A
ENST00000648453.1:c.3559-1G>A	ENSP00000497646.1:n.3559-1G>A
ENST00000680772.1:c.3559-1G>A	ENSP00000506117.1:n.3559-1G>A
ENST00000681142.1:c.3559-1G>A	ENSP00000506682.1:n.3559-1G>A
ENST00000355112.7:c.3559-1G>A	ENSP00000347232.3:n.3559-1G>A
ENST00000558825.5:n.906-1G>A
ENST00000559724.5:c.*2483-1G>A	ENSP00000453359.1:n.*2483-1G>A
ENST00000560136.5:n.1585-1G>A
ENST00000560509.5:c.3359-4971G>A	ENSP00000454158.1:n.3359-4971G>A
NM_000057.3:c.3559-1G>A	NP_000048.1:n.3559-1G>A
NM_001287246.1:c.3559-1G>A	NP_001274175.1:n.3559-1G>A
NM_001287247.1:c.3359-4971G>A	NP_001274176.1:n.3359-4971G>A
NM_001287248.1:c.2434-1G>A	NP_001274177.1:n.2434-1G>A
XM_006720632.2:c.1597-1G>A	XP_006720695.1:n.1597-1G>A
XM_011521881.1:c.2245-1G>A	XP_011520183.1:n.2245-1G>A
XM_011521881.2:c.2245-1G>A	XP_011520183.1:n.2245-1G>A
NM_000057.4:c.3559-1G>A MANE Select	NP_000048.1:n.3559-1G>A
NM_001287246.2:c.3559-1G>A	NP_001274175.1:n.3559-1G>A
NM_001287247.2:c.3359-4971G>A	NP_001274176.1:n.3359-4971G>A
NM_001287248.2:c.2434-1G>A	NP_001274177.1:n.2434-1G>A