Canonical Allele Identifier: CA467877654

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695403G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800951G>A , CM000671.2:g.137800951G>A	GRCh38
NC_000009.11:g.140695403G>A , CM000671.1:g.140695403G>A	GRCh37
NC_000009.10:g.139815224G>A	NCBI36
NG_011776.1:g.186960G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2679G>A MANE Select	ENSP00000417980.1:p.Leu893=
ENST00000636027.1:c.2565G>A	ENSP00000489961.1:p.Leu855=
ENST00000637161.1:c.2586G>A	ENSP00000490328.1:p.Leu862=
ENST00000637261.1:c.2719G>A	ENSP00000490815.1:n.2719G>A
ENST00000637891.1:c.573G>A	ENSP00000490907.1:p.Leu191=
ENST00000637949.1:c.357G>A	ENSP00000489786.1:p.Leu119=
ENST00000460843.5:c.2679G>A	ENSP00000417980.1:p.Leu893=
ENST00000462942.3:c.1536G>A	ENSP00000436107.1:p.Leu512=
ENST00000482340.5:c.249G>A	ENSP00000486748.1:p.Leu83=
ENST00000486164.5:c.257G>A
ENST00000488242.2:n.205G>A
ENST00000493484.5:c.249G>A	ENSP00000486503.1:p.Leu83=
NM_024757.4:c.2679G>A	NP_079033.4:p.Leu893=
XM_005266105.3:c.2670G>A	XP_005266162.1:p.Leu890=
XM_005266110.1:c.2586G>A	XP_005266167.1:p.Leu862=
XM_006717288.2:c.2661G>A	XP_006717351.1:p.Leu887=
XM_011519021.1:c.2688G>A	XP_011517323.1:p.Leu896=
XM_011519022.1:c.2685G>A	XP_011517324.1:p.Leu895=
XM_011519023.1:c.2667G>A	XP_011517325.1:p.Leu889=
XM_011519024.1:c.2610G>A	XP_011517326.1:p.Leu870=
XM_011519025.1:c.2586G>A	XP_011517327.1:p.Leu862=
XM_011519026.1:c.2544G>A	XP_011517328.1:p.Leu848=
XM_011519027.1:c.2688G>A	XP_011517329.1:p.Leu896=
XM_011519029.1:c.1110G>A	XP_011517331.1:p.Leu370=
XM_011519030.1:c.462G>A	XP_011517332.1:p.Leu154=
XM_011519031.1:c.249G>A	XP_011517333.1:p.Leu83=
XM_011519032.1:c.249G>A	XP_011517334.1:p.Leu83=
XM_011519033.1:c.2523G>A	XP_011517335.1:p.Leu841=
NM_001354263.1:c.2658G>A	NP_001341192.1:p.Leu886=
XM_005266105.5:c.2670G>A	XP_005266162.1:p.Leu890=
XM_011519021.3:c.2688G>A	XP_011517323.1:p.Leu896=
XM_011519022.3:c.2685G>A	XP_011517324.1:p.Leu895=
XM_011519023.3:c.2667G>A	XP_011517325.1:p.Leu889=
XM_011519029.3:c.1110G>A	XP_011517331.1:p.Leu370=
XM_011519030.3:c.462G>A	XP_011517332.1:p.Leu154=
XM_017015134.1:c.2664G>A	XP_016870623.1:p.Leu888=
XM_017015136.2:c.2580G>A	XP_016870625.1:p.Leu860=
XM_017015137.1:c.2565G>A	XP_016870626.1:p.Leu855=
XM_017015138.1:c.2565G>A	XP_016870627.1:p.Leu855=
XM_024447674.1:c.2508G>A	XP_024303442.1:p.Leu836=
XM_024447675.1:c.2442G>A	XP_024303443.1:p.Leu814=
XM_024447676.1:c.1803G>A	XP_024303444.1:p.Leu601=
XM_024447677.1:c.1803G>A	XP_024303445.1:p.Leu601=
XM_024447678.1:c.2586G>A	XP_024303446.1:p.Leu862=
XM_024447680.1:c.2421G>A	XP_024303448.1:p.Leu807=
NM_024757.5:c.2679G>A MANE Select	NP_079033.4:p.Leu893=
NM_001354263.2:c.2658G>A	NP_001341192.1:p.Leu886=