Canonical Allele Identifier: CA468161085

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707575G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813123G>C , CM000671.2:g.137813123G>C	GRCh38
NC_000009.11:g.140707575G>C , CM000671.1:g.140707575G>C	GRCh37
NC_000009.10:g.139827396G>C	NCBI36
NG_011776.1:g.199132G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2985G>C MANE Select	ENSP00000417980.1:p.Leu995=
ENST00000636027.1:c.2871G>C	ENSP00000489961.1:p.Leu957=
ENST00000637161.1:c.2892G>C	ENSP00000490328.1:p.Leu964=
ENST00000637261.1:c.3025G>C	ENSP00000490815.1:n.3025G>C
ENST00000637891.1:c.879G>C	ENSP00000490907.1:p.Leu293=
ENST00000460843.5:c.2985G>C	ENSP00000417980.1:p.Leu995=
ENST00000462942.3:c.1842G>C	ENSP00000436107.1:p.Leu614=
ENST00000486164.5:c.672G>C
ENST00000488242.2:n.511G>C
NM_024757.4:c.2985G>C	NP_079033.4:p.Leu995=
XM_005266105.3:c.2976G>C	XP_005266162.1:p.Leu992=
XM_005266110.1:c.2892G>C	XP_005266167.1:p.Leu964=
XM_006717288.2:c.2967G>C	XP_006717351.1:p.Leu989=
XM_011519021.1:c.2994G>C	XP_011517323.1:p.Leu998=
XM_011519022.1:c.2991G>C	XP_011517324.1:p.Leu997=
XM_011519023.1:c.2973G>C	XP_011517325.1:p.Leu991=
XM_011519024.1:c.2916G>C	XP_011517326.1:p.Leu972=
XM_011519025.1:c.2892G>C	XP_011517327.1:p.Leu964=
XM_011519026.1:c.2850G>C	XP_011517328.1:p.Leu950=
XM_011519029.1:c.1416G>C	XP_011517331.1:p.Leu472=
XM_011519030.1:c.768G>C	XP_011517332.1:p.Leu256=
XM_011519031.1:c.555G>C	XP_011517333.1:p.Leu185=
XM_011519032.1:c.555G>C	XP_011517334.1:p.Leu185=
XM_011519033.1:c.2829G>C	XP_011517335.1:p.Leu943=
NM_001354263.1:c.2964G>C	NP_001341192.1:p.Leu988=
XM_005266105.5:c.2976G>C	XP_005266162.1:p.Leu992=
XM_011519021.3:c.2994G>C	XP_011517323.1:p.Leu998=
XM_011519022.3:c.2991G>C	XP_011517324.1:p.Leu997=
XM_011519023.3:c.2973G>C	XP_011517325.1:p.Leu991=
XM_011519029.3:c.1416G>C	XP_011517331.1:p.Leu472=
XM_011519030.3:c.768G>C	XP_011517332.1:p.Leu256=
XM_017015134.1:c.2970G>C	XP_016870623.1:p.Leu990=
XM_017015136.2:c.2886G>C	XP_016870625.1:p.Leu962=
XM_017015137.1:c.2871G>C	XP_016870626.1:p.Leu957=
XM_017015138.1:c.2871G>C	XP_016870627.1:p.Leu957=
XM_024447674.1:c.2814G>C	XP_024303442.1:p.Leu938=
XM_024447675.1:c.2748G>C	XP_024303443.1:p.Leu916=
XM_024447676.1:c.2109G>C	XP_024303444.1:p.Leu703=
XM_024447677.1:c.2109G>C	XP_024303445.1:p.Leu703=
XM_024447680.1:c.2727G>C	XP_024303448.1:p.Leu909=
NM_024757.5:c.2985G>C MANE Select	NP_079033.4:p.Leu995=
NM_001354263.2:c.2964G>C	NP_001341192.1:p.Leu988=