Canonical Allele Identifier: CA2580090512

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90765282T>G , CM000677.2:g.90765282T>G	GRCh38
NC_000015.9:g.91308512T>G , CM000677.1:g.91308512T>G	GRCh37
NC_000015.8:g.89109516T>G	NCBI36
NG_007272.1:g.52911T>G , LRG_20:g.52911T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000057.4:c.2075-14T>G MANE Select	NP_000048.1:n.2075-14T>G
ENST00000355112.8:c.2075-14T>G MANE Select	ENSP00000347232.3:n.2075-14T>G
NM_000057.3:c.2075-14T>G	NP_000048.1:n.2075-14T>G
NM_001287246.1:c.2075-14T>G	NP_001274175.1:n.2075-14T>G
NM_001287246.2:c.2075-14T>G	NP_001274175.1:n.2075-14T>G
NM_001287247.1:c.2075-14T>G	NP_001274176.1:n.2075-14T>G
NM_001287247.2:c.2075-14T>G	NP_001274176.1:n.2075-14T>G
NM_001287248.1:c.950-14T>G	NP_001274177.1:n.950-14T>G
NM_001287248.2:c.950-14T>G	NP_001274177.1:n.950-14T>G
ENST00000355112.7:c.2075-14T>G	ENSP00000347232.3:n.2075-14T>G
ENST00000559426.5:n.252-14T>G
ENST00000559724.5:c.*999-14T>G	ENSP00000453359.1:n.*999-14T>G
ENST00000560136.5:n.220-1628T>G
ENST00000560509.5:c.2075-14T>G	ENSP00000454158.1:n.2075-14T>G
ENST00000648453.1:c.2075-14T>G	ENSP00000497646.1:n.2075-14T>G
ENST00000680772.1:c.2075-14T>G	ENSP00000506117.1:n.2075-14T>G
ENST00000681142.1:c.2075-14T>G	ENSP00000506682.1:n.2075-14T>G
XM_006720632.2:c.113-14T>G	XP_006720695.1:n.113-14T>G
XM_011521881.1:c.761-14T>G	XP_011520183.1:n.761-14T>G
XM_011521881.2:c.761-14T>G	XP_011520183.1:n.761-14T>G
XM_011521882.1:c.2075-14T>G	XP_011520184.1:n.2075-14T>G
XM_011521882.3:c.2075-14T>G	XP_011520184.1:n.2075-14T>G