Canonical Allele Identifier: CA2318160632

Gene: DOT1L

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2176587A>C , CM000681.2:g.2176587A>C	GRCh38
NC_000019.9:g.2176586A>C , CM000681.1:g.2176586A>C	GRCh37
NC_000019.8:g.2127586A>C	NCBI36
NG_029793.1:g.17439A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686010.1:c.82-4126A>C	ENSP00000510335.1:n.82-4126A>C
ENST00000398665.8:c.82-4126A>C MANE Select	ENSP00000381657.3:n.82-4126A>C
ENST00000398665.7:c.82-4126A>C	ENSP00000381657.3:n.82-4126A>C
ENST00000452696.5:c.82-4126A>C	ENSP00000404284.1:n.82-4126A>C
ENST00000478937.3:c.69-4126A>C
NM_032482.2:c.82-4126A>C	NP_115871.1:n.82-4126A>C
XM_005259659.2:c.82-4126A>C	XP_005259716.1:n.82-4126A>C
XM_005259660.2:c.82-4126A>C	XP_005259717.1:n.82-4126A>C
XM_006722923.2:c.-539-4126A>C	XP_006722986.1:n.-539-4126A>C
XM_011528359.1:c.82-4126A>C	XP_011526661.1:n.82-4126A>C
XM_011528360.1:c.-222-4126A>C	XP_011526662.1:n.-222-4126A>C
XM_005259659.3:c.82-4126A>C	XP_005259716.1:n.82-4126A>C
XM_005259660.3:c.82-4126A>C	XP_005259717.1:n.82-4126A>C
XM_011528359.2:c.82-4126A>C	XP_011526661.1:n.82-4126A>C
XM_017027366.1:c.-539-4126A>C	XP_016882855.1:n.-539-4126A>C
NM_032482.3:c.82-4126A>C MANE Select	NP_115871.1:n.82-4126A>C