Canonical Allele Identifier: CA375788808

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695362G>T (hg19) ; chr9:g.137800910G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800910G>T , CM000671.2:g.137800910G>T	GRCh38
NC_000009.11:g.140695362G>T , CM000671.1:g.140695362G>T	GRCh37
NC_000009.10:g.139815183G>T	NCBI36
NG_011776.1:g.186919G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2638G>T MANE Select	ENSP00000417980.1:p.Ala880Ser
ENST00000636027.1:c.2524G>T	ENSP00000489961.1:p.Ala842Ser
ENST00000637161.1:c.2545G>T	ENSP00000490328.1:p.Ala849Ser
ENST00000637261.1:c.2678G>T	ENSP00000490815.1:n.2678G>T
ENST00000637891.1:c.532G>T	ENSP00000490907.1:p.Ala178Ser
ENST00000637949.1:c.316G>T	ENSP00000489786.1:p.Ala106Ser
ENST00000460843.5:c.2638G>T	ENSP00000417980.1:p.Ala880Ser
ENST00000462942.3:c.1495G>T	ENSP00000436107.1:p.Ala499Ser
ENST00000482340.5:c.208G>T	ENSP00000486748.1:p.Ala70Ser
ENST00000486164.5:c.216G>T
ENST00000488242.2:n.164G>T
ENST00000493484.5:c.208G>T	ENSP00000486503.1:p.Ala70Ser
NM_024757.4:c.2638G>T	NP_079033.4:p.Ala880Ser
XM_005266105.3:c.2629G>T	XP_005266162.1:p.Ala877Ser
XM_005266110.1:c.2545G>T	XP_005266167.1:p.Ala849Ser
XM_006717288.2:c.2620G>T	XP_006717351.1:p.Ala874Ser
XM_011519021.1:c.2647G>T	XP_011517323.1:p.Ala883Ser
XM_011519022.1:c.2644G>T	XP_011517324.1:p.Ala882Ser
XM_011519023.1:c.2626G>T	XP_011517325.1:p.Ala876Ser
XM_011519024.1:c.2569G>T	XP_011517326.1:p.Ala857Ser
XM_011519025.1:c.2545G>T	XP_011517327.1:p.Ala849Ser
XM_011519026.1:c.2503G>T	XP_011517328.1:p.Ala835Ser
XM_011519027.1:c.2647G>T	XP_011517329.1:p.Ala883Ser
XM_011519029.1:c.1069G>T	XP_011517331.1:p.Ala357Ser
XM_011519030.1:c.421G>T	XP_011517332.1:p.Ala141Ser
XM_011519031.1:c.208G>T	XP_011517333.1:p.Ala70Ser
XM_011519032.1:c.208G>T	XP_011517334.1:p.Ala70Ser
XM_011519033.1:c.2482G>T	XP_011517335.1:p.Ala828Ser
NM_001354263.1:c.2617G>T	NP_001341192.1:p.Ala873Ser
XM_005266105.5:c.2629G>T	XP_005266162.1:p.Ala877Ser
XM_011519021.3:c.2647G>T	XP_011517323.1:p.Ala883Ser
XM_011519022.3:c.2644G>T	XP_011517324.1:p.Ala882Ser
XM_011519023.3:c.2626G>T	XP_011517325.1:p.Ala876Ser
XM_011519029.3:c.1069G>T	XP_011517331.1:p.Ala357Ser
XM_011519030.3:c.421G>T	XP_011517332.1:p.Ala141Ser
XM_017015134.1:c.2623G>T	XP_016870623.1:p.Ala875Ser
XM_017015136.2:c.2539G>T	XP_016870625.1:p.Ala847Ser
XM_017015137.1:c.2524G>T	XP_016870626.1:p.Ala842Ser
XM_017015138.1:c.2524G>T	XP_016870627.1:p.Ala842Ser
XM_024447674.1:c.2467G>T	XP_024303442.1:p.Ala823Ser
XM_024447675.1:c.2401G>T	XP_024303443.1:p.Ala801Ser
XM_024447676.1:c.1762G>T	XP_024303444.1:p.Ala588Ser
XM_024447677.1:c.1762G>T	XP_024303445.1:p.Ala588Ser
XM_024447678.1:c.2545G>T	XP_024303446.1:p.Ala849Ser
XM_024447680.1:c.2380G>T	XP_024303448.1:p.Ala794Ser
NM_024757.5:c.2638G>T MANE Select	NP_079033.4:p.Ala880Ser
NM_001354263.2:c.2617G>T	NP_001341192.1:p.Ala873Ser