Canonical Allele Identifier: CA344522

Gene: BLM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90794338A>T , CM000677.2:g.90794338A>T	GRCh38
NC_000015.9:g.91337568A>T , CM000677.1:g.91337568A>T	GRCh37
NC_000015.8:g.89138572A>T	NCBI36
NG_007272.1:g.81967A>T , LRG_20:g.81967A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000057.4:c.3191A>T MANE Select	NP_000048.1:p.Asp1064Val
ENST00000355112.8:c.3191A>T MANE Select	ENSP00000347232.3:p.Asp1064Val
NM_000057.3:c.3191A>T	NP_000048.1:p.Asp1064Val
NM_001287246.1:c.3191A>T	NP_001274175.1:p.Asp1064Val
NM_001287246.2:c.3191A>T	NP_001274175.1:p.Asp1064Val
NM_001287247.1:c.3191A>T	NP_001274176.1:p.Asp1064Val
NM_001287247.2:c.3191A>T	NP_001274176.1:p.Asp1064Val
NM_001287248.1:c.2066A>T	NP_001274177.1:p.Asp689Val
NM_001287248.2:c.2066A>T	NP_001274177.1:p.Asp689Val
ENST00000355112.7:c.3191A>T	ENSP00000347232.3:p.Asp1064Val
ENST00000558825.5:n.538A>T
ENST00000559724.5:c.*2115A>T	ENSP00000453359.1:n.*2115A>T
ENST00000560136.5:n.1217A>T
ENST00000560509.5:c.3191A>T	ENSP00000454158.1:p.Asp1064Val
ENST00000560559.1:n.728A>T
ENST00000560559.2:n.1764A>T
ENST00000648453.1:c.3191A>T	ENSP00000497646.1:p.Asp1064Val
ENST00000680772.1:c.3191A>T	ENSP00000506117.1:p.Asp1064Val
ENST00000681142.1:c.3191A>T	ENSP00000506682.1:p.Asp1064Val
XM_006720632.2:c.1229A>T	XP_006720695.1:p.Asp410Val
XM_011521881.1:c.1877A>T	XP_011520183.1:p.Asp626Val
XM_011521881.2:c.1877A>T	XP_011520183.1:p.Asp626Val