Canonical Allele Identifier: CA2318171132

Gene: DOT1L

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2194897T= , CM000681.2:g.2194897T=	GRCh38
NC_000019.9:g.2194896T= , CM000681.1:g.2194896T=	GRCh37
NC_000019.8:g.2145896T=	NCBI36
NG_029793.1:g.35749T=

Transcript Alleles

HGVS	Amino-acid Change
NM_032482.3:c.651+320T= MANE Select	NP_115871.1:n.651+320T=
ENST00000398665.8:c.651+320T= MANE Select	ENSP00000381657.3:n.651+320T=
NM_032482.2:c.651+320T=	NP_115871.1:n.651+320T=
ENST00000398665.7:c.651+320T=	ENSP00000381657.3:n.651+320T=
ENST00000452696.5:c.579+320T=	ENSP00000404284.1:n.579+320T=
ENST00000686010.1:c.651+320T=	ENSP00000510335.1:n.651+320T=
XM_005259659.2:c.651+320T=	XP_005259716.1:n.651+320T=
XM_005259659.3:c.651+320T=	XP_005259716.1:n.651+320T=
XM_005259660.2:c.651+320T=	XP_005259717.1:n.651+320T=
XM_005259660.3:c.651+320T=	XP_005259717.1:n.651+320T=
XM_006722923.2:c.31+320T=	XP_006722986.1:n.31+320T=
XM_011528359.1:c.651+320T=	XP_011526661.1:n.651+320T=
XM_011528359.2:c.651+320T=	XP_011526661.1:n.651+320T=
XM_011528360.1:c.441+320T=	XP_011526662.1:n.441+320T=
XM_017027366.1:c.31+320T=	XP_016882855.1:n.31+320T=