Canonical Allele Identifier: CA375793577

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707562T>G (hg19) ; chr9:g.137813110T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813110T>G , CM000671.2:g.137813110T>G	GRCh38
NC_000009.11:g.140707562T>G , CM000671.1:g.140707562T>G	GRCh37
NC_000009.10:g.139827383T>G	NCBI36
NG_011776.1:g.199119T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2972T>G MANE Select	ENSP00000417980.1:p.Met991Arg
ENST00000636027.1:c.2858T>G	ENSP00000489961.1:p.Met953Arg
ENST00000637161.1:c.2879T>G	ENSP00000490328.1:p.Met960Arg
ENST00000637261.1:c.3012T>G	ENSP00000490815.1:n.3012T>G
ENST00000637891.1:c.866T>G	ENSP00000490907.1:p.Met289Arg
ENST00000460843.5:c.2972T>G	ENSP00000417980.1:p.Met991Arg
ENST00000462942.3:c.1829T>G	ENSP00000436107.1:p.Met610Arg
ENST00000486164.5:c.659T>G
ENST00000488242.2:n.498T>G
NM_024757.4:c.2972T>G	NP_079033.4:p.Met991Arg
XM_005266105.3:c.2963T>G	XP_005266162.1:p.Met988Arg
XM_005266110.1:c.2879T>G	XP_005266167.1:p.Met960Arg
XM_006717288.2:c.2954T>G	XP_006717351.1:p.Met985Arg
XM_011519021.1:c.2981T>G	XP_011517323.1:p.Met994Arg
XM_011519022.1:c.2978T>G	XP_011517324.1:p.Met993Arg
XM_011519023.1:c.2960T>G	XP_011517325.1:p.Met987Arg
XM_011519024.1:c.2903T>G	XP_011517326.1:p.Met968Arg
XM_011519025.1:c.2879T>G	XP_011517327.1:p.Met960Arg
XM_011519026.1:c.2837T>G	XP_011517328.1:p.Met946Arg
XM_011519029.1:c.1403T>G	XP_011517331.1:p.Met468Arg
XM_011519030.1:c.755T>G	XP_011517332.1:p.Met252Arg
XM_011519031.1:c.542T>G	XP_011517333.1:p.Met181Arg
XM_011519032.1:c.542T>G	XP_011517334.1:p.Met181Arg
XM_011519033.1:c.2816T>G	XP_011517335.1:p.Met939Arg
NM_001354263.1:c.2951T>G	NP_001341192.1:p.Met984Arg
XM_005266105.5:c.2963T>G	XP_005266162.1:p.Met988Arg
XM_011519021.3:c.2981T>G	XP_011517323.1:p.Met994Arg
XM_011519022.3:c.2978T>G	XP_011517324.1:p.Met993Arg
XM_011519023.3:c.2960T>G	XP_011517325.1:p.Met987Arg
XM_011519029.3:c.1403T>G	XP_011517331.1:p.Met468Arg
XM_011519030.3:c.755T>G	XP_011517332.1:p.Met252Arg
XM_017015134.1:c.2957T>G	XP_016870623.1:p.Met986Arg
XM_017015136.2:c.2873T>G	XP_016870625.1:p.Met958Arg
XM_017015137.1:c.2858T>G	XP_016870626.1:p.Met953Arg
XM_017015138.1:c.2858T>G	XP_016870627.1:p.Met953Arg
XM_024447674.1:c.2801T>G	XP_024303442.1:p.Met934Arg
XM_024447675.1:c.2735T>G	XP_024303443.1:p.Met912Arg
XM_024447676.1:c.2096T>G	XP_024303444.1:p.Met699Arg
XM_024447677.1:c.2096T>G	XP_024303445.1:p.Met699Arg
XM_024447680.1:c.2714T>G	XP_024303448.1:p.Met905Arg
NM_024757.5:c.2972T>G MANE Select	NP_079033.4:p.Met991Arg
NM_001354263.2:c.2951T>G	NP_001341192.1:p.Met984Arg