Canonical Allele Identifier: CA375793700

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707603C>T (hg19) ; chr9:g.137813151C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813151C>T , CM000671.2:g.137813151C>T	GRCh38
NC_000009.11:g.140707603C>T , CM000671.1:g.140707603C>T	GRCh37
NC_000009.10:g.139827424C>T	NCBI36
NG_011776.1:g.199160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3013C>T MANE Select	ENSP00000417980.1:p.Pro1005Ser
ENST00000636027.1:c.2899C>T	ENSP00000489961.1:p.Pro967Ser
ENST00000637161.1:c.2920C>T	ENSP00000490328.1:p.Pro974Ser
ENST00000637261.1:c.3053C>T	ENSP00000490815.1:n.3053C>T
ENST00000637891.1:c.907C>T	ENSP00000490907.1:p.Pro303Ser
ENST00000460843.5:c.3013C>T	ENSP00000417980.1:p.Pro1005Ser
ENST00000462942.3:c.1870C>T	ENSP00000436107.1:p.Pro624Ser
ENST00000486164.5:c.700C>T
ENST00000488242.2:n.539C>T
NM_024757.4:c.3013C>T	NP_079033.4:p.Pro1005Ser
XM_005266105.3:c.3004C>T	XP_005266162.1:p.Pro1002Ser
XM_005266110.1:c.2920C>T	XP_005266167.1:p.Pro974Ser
XM_006717288.2:c.2995C>T	XP_006717351.1:p.Pro999Ser
XM_011519021.1:c.3022C>T	XP_011517323.1:p.Pro1008Ser
XM_011519022.1:c.3019C>T	XP_011517324.1:p.Pro1007Ser
XM_011519023.1:c.3001C>T	XP_011517325.1:p.Pro1001Ser
XM_011519024.1:c.2944C>T	XP_011517326.1:p.Pro982Ser
XM_011519025.1:c.2920C>T	XP_011517327.1:p.Pro974Ser
XM_011519026.1:c.2878C>T	XP_011517328.1:p.Pro960Ser
XM_011519029.1:c.1444C>T	XP_011517331.1:p.Pro482Ser
XM_011519030.1:c.796C>T	XP_011517332.1:p.Pro266Ser
XM_011519031.1:c.583C>T	XP_011517333.1:p.Pro195Ser
XM_011519032.1:c.583C>T	XP_011517334.1:p.Pro195Ser
XM_011519033.1:c.2857C>T	XP_011517335.1:p.Pro953Ser
NM_001354263.1:c.2992C>T	NP_001341192.1:p.Pro998Ser
XM_005266105.5:c.3004C>T	XP_005266162.1:p.Pro1002Ser
XM_011519021.3:c.3022C>T	XP_011517323.1:p.Pro1008Ser
XM_011519022.3:c.3019C>T	XP_011517324.1:p.Pro1007Ser
XM_011519023.3:c.3001C>T	XP_011517325.1:p.Pro1001Ser
XM_011519029.3:c.1444C>T	XP_011517331.1:p.Pro482Ser
XM_011519030.3:c.796C>T	XP_011517332.1:p.Pro266Ser
XM_017015134.1:c.2998C>T	XP_016870623.1:p.Pro1000Ser
XM_017015136.2:c.2914C>T	XP_016870625.1:p.Pro972Ser
XM_017015137.1:c.2899C>T	XP_016870626.1:p.Pro967Ser
XM_017015138.1:c.2899C>T	XP_016870627.1:p.Pro967Ser
XM_024447674.1:c.2842C>T	XP_024303442.1:p.Pro948Ser
XM_024447675.1:c.2776C>T	XP_024303443.1:p.Pro926Ser
XM_024447676.1:c.2137C>T	XP_024303444.1:p.Pro713Ser
XM_024447677.1:c.2137C>T	XP_024303445.1:p.Pro713Ser
XM_024447680.1:c.2755C>T	XP_024303448.1:p.Pro919Ser
NM_024757.5:c.3013C>T MANE Select	NP_079033.4:p.Pro1005Ser
NM_001354263.2:c.2992C>T	NP_001341192.1:p.Pro998Ser