Canonical Allele Identifier: CA2630381785

Gene: BLM

Linked Data

• gnomAD v4: 15-90790893-ATAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90790898_90790900del , CM000677.2:g.90790898_90790900del	GRCh38
NC_000015.9:g.91334128_91334130del , CM000677.1:g.91334128_91334130del	GRCh37
NC_000015.8:g.89135132_89135134del	NCBI36
NG_007272.1:g.78527_78529del , LRG_20:g.78527_78529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3019+54_3019+56del MANE Select	ENSP00000347232.3:n.3019+54_3019+56del
ENST00000560559.2:n.1592+54_1592+56del
ENST00000648453.1:c.3019+54_3019+56del	ENSP00000497646.1:n.3019+54_3019+56del
ENST00000680772.1:c.3019+54_3019+56del	ENSP00000506117.1:n.3019+54_3019+56del
ENST00000681142.1:c.3019+54_3019+56del	ENSP00000506682.1:n.3019+54_3019+56del
ENST00000355112.7:c.3019+54_3019+56del	ENSP00000347232.3:n.3019+54_3019+56del
ENST00000559724.5:c.*1943+54_*1943+56del	ENSP00000453359.1:n.*1943+54_*1943+56del
ENST00000560136.5:n.1045+54_1045+56del
ENST00000560509.5:c.3019+54_3019+56del	ENSP00000454158.1:n.3019+54_3019+56del
ENST00000560559.1:n.556+54_556+56del
NM_000057.3:c.3019+54_3019+56del	NP_000048.1:n.3019+54_3019+56del
NM_001287246.1:c.3019+54_3019+56del	NP_001274175.1:n.3019+54_3019+56del
NM_001287247.1:c.3019+54_3019+56del	NP_001274176.1:n.3019+54_3019+56del
NM_001287248.1:c.1894+54_1894+56del	NP_001274177.1:n.1894+54_1894+56del
XM_006720632.2:c.1057+54_1057+56del	XP_006720695.1:n.1057+54_1057+56del
XM_011521881.1:c.1705+54_1705+56del	XP_011520183.1:n.1705+54_1705+56del
XM_011521881.2:c.1705+54_1705+56del	XP_011520183.1:n.1705+54_1705+56del
NM_000057.4:c.3019+54_3019+56del MANE Select	NP_000048.1:n.3019+54_3019+56del
NM_001287246.2:c.3019+54_3019+56del	NP_001274175.1:n.3019+54_3019+56del
NM_001287247.2:c.3019+54_3019+56del	NP_001274176.1:n.3019+54_3019+56del
NM_001287248.2:c.1894+54_1894+56del	NP_001274177.1:n.1894+54_1894+56del