Canonical Allele Identifier: CA14694887

Gene: DOT1L

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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