Canonical Allele Identifier: CA393849828

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90809248G>A , CM000677.2:g.90809248G>A	GRCh38
NC_000015.9:g.91352478G>A , CM000677.1:g.91352478G>A	GRCh37
NC_000015.8:g.89153482G>A	NCBI36
NG_007272.1:g.96877G>A , LRG_20:g.96877G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000057.4:c.3863G>A MANE Select	NP_000048.1:p.Trp1288Ter
ENST00000355112.8:c.3863G>A MANE Select	ENSP00000347232.3:p.Trp1288Ter
NM_000057.3:c.3863G>A	NP_000048.1:p.Trp1288Ter
NM_001287246.1:c.3863G>A	NP_001274175.1:p.Trp1288Ter
NM_001287246.2:c.3863G>A	NP_001274175.1:p.Trp1288Ter
NM_001287247.1:c.3470G>A	NP_001274176.1:p.Trp1157Ter
NM_001287247.2:c.3470G>A	NP_001274176.1:p.Trp1157Ter
NM_001287248.1:c.2738G>A	NP_001274177.1:p.Trp913Ter
NM_001287248.2:c.2738G>A	NP_001274177.1:p.Trp913Ter
ENST00000355112.7:c.3863G>A	ENSP00000347232.3:p.Trp1288Ter
ENST00000558825.5:n.1210G>A
ENST00000559724.5:c.*2787G>A	ENSP00000453359.1:n.*2787G>A
ENST00000560136.5:n.1889G>A
ENST00000560509.5:c.3470G>A	ENSP00000454158.1:p.Trp1157Ter
ENST00000560559.2:n.2436G>A
ENST00000560821.1:n.283G>A
ENST00000648453.1:c.3863G>A	ENSP00000497646.1:p.Trp1288Ter
ENST00000680772.1:c.3863G>A	ENSP00000506117.1:p.Trp1288Ter
ENST00000681142.1:c.3863G>A	ENSP00000506682.1:p.Trp1288Ter
XM_006720632.2:c.1901G>A	XP_006720695.1:p.Trp634Ter
XM_011521881.1:c.2549G>A	XP_011520183.1:p.Trp850Ter
XM_011521881.2:c.2549G>A	XP_011520183.1:p.Trp850Ter