Canonical Allele Identifier: CA375788948

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695398C>G (hg19) ; chr9:g.137800946C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800946C>G , CM000671.2:g.137800946C>G	GRCh38
NC_000009.11:g.140695398C>G , CM000671.1:g.140695398C>G	GRCh37
NC_000009.10:g.139815219C>G	NCBI36
NG_011776.1:g.186955C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2674C>G MANE Select	ENSP00000417980.1:p.Leu892Val
ENST00000636027.1:c.2560C>G	ENSP00000489961.1:p.Leu854Val
ENST00000637161.1:c.2581C>G	ENSP00000490328.1:p.Leu861Val
ENST00000637261.1:c.2714C>G	ENSP00000490815.1:n.2714C>G
ENST00000637891.1:c.568C>G	ENSP00000490907.1:p.Leu190Val
ENST00000637949.1:c.352C>G	ENSP00000489786.1:p.Leu118Val
ENST00000460843.5:c.2674C>G	ENSP00000417980.1:p.Leu892Val
ENST00000462942.3:c.1531C>G	ENSP00000436107.1:p.Leu511Val
ENST00000482340.5:c.244C>G	ENSP00000486748.1:p.Leu82Val
ENST00000486164.5:c.252C>G
ENST00000488242.2:n.200C>G
ENST00000493484.5:c.244C>G	ENSP00000486503.1:p.Leu82Val
NM_024757.4:c.2674C>G	NP_079033.4:p.Leu892Val
XM_005266105.3:c.2665C>G	XP_005266162.1:p.Leu889Val
XM_005266110.1:c.2581C>G	XP_005266167.1:p.Leu861Val
XM_006717288.2:c.2656C>G	XP_006717351.1:p.Leu886Val
XM_011519021.1:c.2683C>G	XP_011517323.1:p.Leu895Val
XM_011519022.1:c.2680C>G	XP_011517324.1:p.Leu894Val
XM_011519023.1:c.2662C>G	XP_011517325.1:p.Leu888Val
XM_011519024.1:c.2605C>G	XP_011517326.1:p.Leu869Val
XM_011519025.1:c.2581C>G	XP_011517327.1:p.Leu861Val
XM_011519026.1:c.2539C>G	XP_011517328.1:p.Leu847Val
XM_011519027.1:c.2683C>G	XP_011517329.1:p.Leu895Val
XM_011519029.1:c.1105C>G	XP_011517331.1:p.Leu369Val
XM_011519030.1:c.457C>G	XP_011517332.1:p.Leu153Val
XM_011519031.1:c.244C>G	XP_011517333.1:p.Leu82Val
XM_011519032.1:c.244C>G	XP_011517334.1:p.Leu82Val
XM_011519033.1:c.2518C>G	XP_011517335.1:p.Leu840Val
NM_001354263.1:c.2653C>G	NP_001341192.1:p.Leu885Val
XM_005266105.5:c.2665C>G	XP_005266162.1:p.Leu889Val
XM_011519021.3:c.2683C>G	XP_011517323.1:p.Leu895Val
XM_011519022.3:c.2680C>G	XP_011517324.1:p.Leu894Val
XM_011519023.3:c.2662C>G	XP_011517325.1:p.Leu888Val
XM_011519029.3:c.1105C>G	XP_011517331.1:p.Leu369Val
XM_011519030.3:c.457C>G	XP_011517332.1:p.Leu153Val
XM_017015134.1:c.2659C>G	XP_016870623.1:p.Leu887Val
XM_017015136.2:c.2575C>G	XP_016870625.1:p.Leu859Val
XM_017015137.1:c.2560C>G	XP_016870626.1:p.Leu854Val
XM_017015138.1:c.2560C>G	XP_016870627.1:p.Leu854Val
XM_024447674.1:c.2503C>G	XP_024303442.1:p.Leu835Val
XM_024447675.1:c.2437C>G	XP_024303443.1:p.Leu813Val
XM_024447676.1:c.1798C>G	XP_024303444.1:p.Leu600Val
XM_024447677.1:c.1798C>G	XP_024303445.1:p.Leu600Val
XM_024447678.1:c.2581C>G	XP_024303446.1:p.Leu861Val
XM_024447680.1:c.2416C>G	XP_024303448.1:p.Leu806Val
NM_024757.5:c.2674C>G MANE Select	NP_079033.4:p.Leu892Val
NM_001354263.2:c.2653C>G	NP_001341192.1:p.Leu885Val