Canonical Allele Identifier: CA467877648

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695400G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800948G>A , CM000671.2:g.137800948G>A	GRCh38
NC_000009.11:g.140695400G>A , CM000671.1:g.140695400G>A	GRCh37
NC_000009.10:g.139815221G>A	NCBI36
NG_011776.1:g.186957G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2676G>A MANE Select	ENSP00000417980.1:p.Leu892=
ENST00000636027.1:c.2562G>A	ENSP00000489961.1:p.Leu854=
ENST00000637161.1:c.2583G>A	ENSP00000490328.1:p.Leu861=
ENST00000637261.1:c.2716G>A	ENSP00000490815.1:n.2716G>A
ENST00000637891.1:c.570G>A	ENSP00000490907.1:p.Leu190=
ENST00000637949.1:c.354G>A	ENSP00000489786.1:p.Leu118=
ENST00000460843.5:c.2676G>A	ENSP00000417980.1:p.Leu892=
ENST00000462942.3:c.1533G>A	ENSP00000436107.1:p.Leu511=
ENST00000482340.5:c.246G>A	ENSP00000486748.1:p.Leu82=
ENST00000486164.5:c.254G>A
ENST00000488242.2:n.202G>A
ENST00000493484.5:c.246G>A	ENSP00000486503.1:p.Leu82=
NM_024757.4:c.2676G>A	NP_079033.4:p.Leu892=
XM_005266105.3:c.2667G>A	XP_005266162.1:p.Leu889=
XM_005266110.1:c.2583G>A	XP_005266167.1:p.Leu861=
XM_006717288.2:c.2658G>A	XP_006717351.1:p.Leu886=
XM_011519021.1:c.2685G>A	XP_011517323.1:p.Leu895=
XM_011519022.1:c.2682G>A	XP_011517324.1:p.Leu894=
XM_011519023.1:c.2664G>A	XP_011517325.1:p.Leu888=
XM_011519024.1:c.2607G>A	XP_011517326.1:p.Leu869=
XM_011519025.1:c.2583G>A	XP_011517327.1:p.Leu861=
XM_011519026.1:c.2541G>A	XP_011517328.1:p.Leu847=
XM_011519027.1:c.2685G>A	XP_011517329.1:p.Leu895=
XM_011519029.1:c.1107G>A	XP_011517331.1:p.Leu369=
XM_011519030.1:c.459G>A	XP_011517332.1:p.Leu153=
XM_011519031.1:c.246G>A	XP_011517333.1:p.Leu82=
XM_011519032.1:c.246G>A	XP_011517334.1:p.Leu82=
XM_011519033.1:c.2520G>A	XP_011517335.1:p.Leu840=
NM_001354263.1:c.2655G>A	NP_001341192.1:p.Leu885=
XM_005266105.5:c.2667G>A	XP_005266162.1:p.Leu889=
XM_011519021.3:c.2685G>A	XP_011517323.1:p.Leu895=
XM_011519022.3:c.2682G>A	XP_011517324.1:p.Leu894=
XM_011519023.3:c.2664G>A	XP_011517325.1:p.Leu888=
XM_011519029.3:c.1107G>A	XP_011517331.1:p.Leu369=
XM_011519030.3:c.459G>A	XP_011517332.1:p.Leu153=
XM_017015134.1:c.2661G>A	XP_016870623.1:p.Leu887=
XM_017015136.2:c.2577G>A	XP_016870625.1:p.Leu859=
XM_017015137.1:c.2562G>A	XP_016870626.1:p.Leu854=
XM_017015138.1:c.2562G>A	XP_016870627.1:p.Leu854=
XM_024447674.1:c.2505G>A	XP_024303442.1:p.Leu835=
XM_024447675.1:c.2439G>A	XP_024303443.1:p.Leu813=
XM_024447676.1:c.1800G>A	XP_024303444.1:p.Leu600=
XM_024447677.1:c.1800G>A	XP_024303445.1:p.Leu600=
XM_024447678.1:c.2583G>A	XP_024303446.1:p.Leu861=
XM_024447680.1:c.2418G>A	XP_024303448.1:p.Leu806=
NM_024757.5:c.2676G>A MANE Select	NP_079033.4:p.Leu892=
NM_001354263.2:c.2655G>A	NP_001341192.1:p.Leu885=