Canonical Allele Identifier: CA393851004

Gene: BLM

Linked Data

• MyVariant Identifiers: chr15:g.91354537T>A (hg19) ; chr15:g.90811307T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811307T>A , CM000677.2:g.90811307T>A	GRCh38
NC_000015.9:g.91354537T>A , CM000677.1:g.91354537T>A	GRCh37
NC_000015.8:g.89155541T>A	NCBI36
NG_007272.1:g.98936T>A , LRG_20:g.98936T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3977T>A MANE Select	ENSP00000347232.3:p.Phe1326Tyr
ENST00000560559.2:n.2550T>A
ENST00000648453.1:c.3977T>A	ENSP00000497646.1:p.Phe1326Tyr
ENST00000680772.1:c.3977T>A	ENSP00000506117.1:p.Phe1326Tyr
ENST00000681142.1:c.3977T>A	ENSP00000506682.1:p.Phe1326Tyr
ENST00000355112.7:c.3977T>A	ENSP00000347232.3:p.Phe1326Tyr
ENST00000558825.5:n.1324T>A
ENST00000559724.5:c.*2901T>A	ENSP00000453359.1:n.*2901T>A
ENST00000560136.5:n.2003T>A
ENST00000560509.5:c.3584T>A	ENSP00000454158.1:p.Phe1195Tyr
ENST00000560821.1:n.397T>A
NM_000057.3:c.3977T>A	NP_000048.1:p.Phe1326Tyr
NM_001287246.1:c.3977T>A	NP_001274175.1:p.Phe1326Tyr
NM_001287247.1:c.3584T>A	NP_001274176.1:p.Phe1195Tyr
NM_001287248.1:c.2852T>A	NP_001274177.1:p.Phe951Tyr
XM_006720632.2:c.2015T>A	XP_006720695.1:p.Phe672Tyr
XM_011521881.1:c.2663T>A	XP_011520183.1:p.Phe888Tyr
XM_011521881.2:c.2663T>A	XP_011520183.1:p.Phe888Tyr
NM_000057.4:c.3977T>A MANE Select	NP_000048.1:p.Phe1326Tyr
NM_001287246.2:c.3977T>A	NP_001274175.1:p.Phe1326Tyr
NM_001287247.2:c.3584T>A	NP_001274176.1:p.Phe1195Tyr
NM_001287248.2:c.2852T>A	NP_001274177.1:p.Phe951Tyr