Canonical Allele Identifier: CA375793574

Gene: EHMT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2972T>A MANE Select	ENSP00000417980.1:p.Met991Lys
ENST00000636027.1:c.2858T>A	ENSP00000489961.1:p.Met953Lys
ENST00000637161.1:c.2879T>A	ENSP00000490328.1:p.Met960Lys
ENST00000637261.1:c.3012T>A	ENSP00000490815.1:n.3012T>A
ENST00000637891.1:c.866T>A	ENSP00000490907.1:p.Met289Lys
ENST00000460843.5:c.2972T>A	ENSP00000417980.1:p.Met991Lys
ENST00000462942.3:c.1829T>A	ENSP00000436107.1:p.Met610Lys
ENST00000486164.5:c.659T>A
ENST00000488242.2:n.498T>A
NM_024757.4:c.2972T>A	NP_079033.4:p.Met991Lys
XM_005266105.3:c.2963T>A	XP_005266162.1:p.Met988Lys
XM_005266110.1:c.2879T>A	XP_005266167.1:p.Met960Lys
XM_006717288.2:c.2954T>A	XP_006717351.1:p.Met985Lys
XM_011519021.1:c.2981T>A	XP_011517323.1:p.Met994Lys
XM_011519022.1:c.2978T>A	XP_011517324.1:p.Met993Lys
XM_011519023.1:c.2960T>A	XP_011517325.1:p.Met987Lys
XM_011519024.1:c.2903T>A	XP_011517326.1:p.Met968Lys
XM_011519025.1:c.2879T>A	XP_011517327.1:p.Met960Lys
XM_011519026.1:c.2837T>A	XP_011517328.1:p.Met946Lys
XM_011519029.1:c.1403T>A	XP_011517331.1:p.Met468Lys
XM_011519030.1:c.755T>A	XP_011517332.1:p.Met252Lys
XM_011519031.1:c.542T>A	XP_011517333.1:p.Met181Lys
XM_011519032.1:c.542T>A	XP_011517334.1:p.Met181Lys
XM_011519033.1:c.2816T>A	XP_011517335.1:p.Met939Lys
NM_001354263.1:c.2951T>A	NP_001341192.1:p.Met984Lys
XM_005266105.5:c.2963T>A	XP_005266162.1:p.Met988Lys
XM_011519021.3:c.2981T>A	XP_011517323.1:p.Met994Lys
XM_011519022.3:c.2978T>A	XP_011517324.1:p.Met993Lys
XM_011519023.3:c.2960T>A	XP_011517325.1:p.Met987Lys
XM_011519029.3:c.1403T>A	XP_011517331.1:p.Met468Lys
XM_011519030.3:c.755T>A	XP_011517332.1:p.Met252Lys
XM_017015134.1:c.2957T>A	XP_016870623.1:p.Met986Lys
XM_017015136.2:c.2873T>A	XP_016870625.1:p.Met958Lys
XM_017015137.1:c.2858T>A	XP_016870626.1:p.Met953Lys
XM_017015138.1:c.2858T>A	XP_016870627.1:p.Met953Lys
XM_024447674.1:c.2801T>A	XP_024303442.1:p.Met934Lys
XM_024447675.1:c.2735T>A	XP_024303443.1:p.Met912Lys
XM_024447676.1:c.2096T>A	XP_024303444.1:p.Met699Lys
XM_024447677.1:c.2096T>A	XP_024303445.1:p.Met699Lys
XM_024447680.1:c.2714T>A	XP_024303448.1:p.Met905Lys
NM_024757.5:c.2972T>A MANE Select	NP_079033.4:p.Met991Lys
NM_001354263.2:c.2951T>A	NP_001341192.1:p.Met984Lys