Canonical Allele Identifier: CA274770441

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90798292C>G , CM000677.2:g.90798292C>G	GRCh38
NC_000015.9:g.91341522C>G , CM000677.1:g.91341522C>G	GRCh37
NC_000015.8:g.89142526C>G	NCBI36
NG_007272.1:g.85921C>G , LRG_20:g.85921C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000057.4:c.3313C>G MANE Select	NP_000048.1:p.Pro1105Ala
ENST00000355112.8:c.3313C>G MANE Select	ENSP00000347232.3:p.Pro1105Ala
NM_000057.3:c.3313C>G	NP_000048.1:p.Pro1105Ala
NM_001287246.1:c.3313C>G	NP_001274175.1:p.Pro1105Ala
NM_001287246.2:c.3313C>G	NP_001274175.1:p.Pro1105Ala
NM_001287247.1:c.3313C>G	NP_001274176.1:p.Pro1105Ala
NM_001287247.2:c.3313C>G	NP_001274176.1:p.Pro1105Ala
NM_001287248.1:c.2188C>G	NP_001274177.1:p.Pro730Ala
NM_001287248.2:c.2188C>G	NP_001274177.1:p.Pro730Ala
ENST00000355112.7:c.3313C>G	ENSP00000347232.3:p.Pro1105Ala
ENST00000558825.5:n.660C>G
ENST00000559724.5:c.*2237C>G	ENSP00000453359.1:n.*2237C>G
ENST00000560136.5:n.1339C>G
ENST00000560509.5:c.3313C>G	ENSP00000454158.1:p.Pro1105Ala
ENST00000560559.2:n.1886C>G
ENST00000648453.1:c.3313C>G	ENSP00000497646.1:p.Pro1105Ala
ENST00000680772.1:c.3313C>G	ENSP00000506117.1:p.Pro1105Ala
ENST00000681142.1:c.3313C>G	ENSP00000506682.1:p.Pro1105Ala
XM_006720632.2:c.1351C>G	XP_006720695.1:p.Pro451Ala
XM_011521881.1:c.1999C>G	XP_011520183.1:p.Pro667Ala
XM_011521881.2:c.1999C>G	XP_011520183.1:p.Pro667Ala