Canonical Allele Identifier: CA492165277

Gene: BLM

Linked Data

• MyVariant Identifiers: chr15:g.91346797T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90803567T>C , CM000677.2:g.90803567T>C	GRCh38
NC_000015.9:g.91346797T>C , CM000677.1:g.91346797T>C	GRCh37
NC_000015.8:g.89147801T>C	NCBI36
NG_007272.1:g.91196T>C , LRG_20:g.91196T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355112.8:c.3405T>C MANE Select	ENSP00000347232.3:p.Ser1135=
ENST00000560559.2:n.1978T>C
ENST00000648453.1:c.3405T>C	ENSP00000497646.1:p.Ser1135=
ENST00000680772.1:c.3405T>C	ENSP00000506117.1:p.Ser1135=
ENST00000681142.1:c.3405T>C	ENSP00000506682.1:p.Ser1135=
ENST00000355112.7:c.3405T>C	ENSP00000347232.3:p.Ser1135=
ENST00000558825.5:n.752T>C
ENST00000559724.5:c.*2329T>C	ENSP00000453359.1:n.*2329T>C
ENST00000560136.5:n.1431T>C
ENST00000560509.5:c.3358+5230T>C	ENSP00000454158.1:n.3358+5230T>C
NM_000057.3:c.3405T>C	NP_000048.1:p.Ser1135=
NM_001287246.1:c.3405T>C	NP_001274175.1:p.Ser1135=
NM_001287247.1:c.3358+5230T>C	NP_001274176.1:n.3358+5230T>C
NM_001287248.1:c.2280T>C	NP_001274177.1:p.Ser760=
XM_006720632.2:c.1443T>C	XP_006720695.1:p.Ser481=
XM_011521881.1:c.2091T>C	XP_011520183.1:p.Ser697=
XM_011521881.2:c.2091T>C	XP_011520183.1:p.Ser697=
NM_000057.4:c.3405T>C MANE Select	NP_000048.1:p.Ser1135=
NM_001287246.2:c.3405T>C	NP_001274175.1:p.Ser1135=
NM_001287247.2:c.3358+5230T>C	NP_001274176.1:n.3358+5230T>C
NM_001287248.2:c.2280T>C	NP_001274177.1:p.Ser760=