Canonical Allele Identifier: CA375793190

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707466T>A (hg19) ; chr9:g.137813014T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813014T>A , CM000671.2:g.137813014T>A	GRCh38
NC_000009.11:g.140707466T>A , CM000671.1:g.140707466T>A	GRCh37
NC_000009.10:g.139827287T>A	NCBI36
NG_011776.1:g.199023T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2876T>A MANE Select	ENSP00000417980.1:p.Leu959His
ENST00000636027.1:c.2762T>A	ENSP00000489961.1:p.Leu921His
ENST00000637161.1:c.2783T>A	ENSP00000490328.1:p.Leu928His
ENST00000637261.1:c.2916T>A	ENSP00000490815.1:n.2916T>A
ENST00000637891.1:c.770T>A	ENSP00000490907.1:p.Leu257His
ENST00000460843.5:c.2876T>A	ENSP00000417980.1:p.Leu959His
ENST00000462942.3:c.1733T>A	ENSP00000436107.1:p.Leu578His
ENST00000486164.5:c.563T>A
ENST00000488242.2:n.402T>A
NM_024757.4:c.2876T>A	NP_079033.4:p.Leu959His
XM_005266105.3:c.2867T>A	XP_005266162.1:p.Leu956His
XM_005266110.1:c.2783T>A	XP_005266167.1:p.Leu928His
XM_006717288.2:c.2858T>A	XP_006717351.1:p.Leu953His
XM_011519021.1:c.2885T>A	XP_011517323.1:p.Leu962His
XM_011519022.1:c.2882T>A	XP_011517324.1:p.Leu961His
XM_011519023.1:c.2864T>A	XP_011517325.1:p.Leu955His
XM_011519024.1:c.2807T>A	XP_011517326.1:p.Leu936His
XM_011519025.1:c.2783T>A	XP_011517327.1:p.Leu928His
XM_011519026.1:c.2741T>A	XP_011517328.1:p.Leu914His
XM_011519029.1:c.1307T>A	XP_011517331.1:p.Leu436His
XM_011519030.1:c.659T>A	XP_011517332.1:p.Leu220His
XM_011519031.1:c.446T>A	XP_011517333.1:p.Leu149His
XM_011519032.1:c.446T>A	XP_011517334.1:p.Leu149His
XM_011519033.1:c.2720T>A	XP_011517335.1:p.Leu907His
NM_001354263.1:c.2855T>A	NP_001341192.1:p.Leu952His
XM_005266105.5:c.2867T>A	XP_005266162.1:p.Leu956His
XM_011519021.3:c.2885T>A	XP_011517323.1:p.Leu962His
XM_011519022.3:c.2882T>A	XP_011517324.1:p.Leu961His
XM_011519023.3:c.2864T>A	XP_011517325.1:p.Leu955His
XM_011519029.3:c.1307T>A	XP_011517331.1:p.Leu436His
XM_011519030.3:c.659T>A	XP_011517332.1:p.Leu220His
XM_017015134.1:c.2861T>A	XP_016870623.1:p.Leu954His
XM_017015136.2:c.2777T>A	XP_016870625.1:p.Leu926His
XM_017015137.1:c.2762T>A	XP_016870626.1:p.Leu921His
XM_017015138.1:c.2762T>A	XP_016870627.1:p.Leu921His
XM_024447674.1:c.2705T>A	XP_024303442.1:p.Leu902His
XM_024447675.1:c.2639T>A	XP_024303443.1:p.Leu880His
XM_024447676.1:c.2000T>A	XP_024303444.1:p.Leu667His
XM_024447677.1:c.2000T>A	XP_024303445.1:p.Leu667His
XM_024447680.1:c.2618T>A	XP_024303448.1:p.Leu873His
NM_024757.5:c.2876T>A MANE Select	NP_079033.4:p.Leu959His
NM_001354263.2:c.2855T>A	NP_001341192.1:p.Leu952His