Canonical Allele Identifier: CA375788978

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695408A>T (hg19) ; chr9:g.137800956A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800956A>T , CM000671.2:g.137800956A>T	GRCh38
NC_000009.11:g.140695408A>T , CM000671.1:g.140695408A>T	GRCh37
NC_000009.10:g.139815229A>T	NCBI36
NG_011776.1:g.186965A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2684A>T MANE Select	ENSP00000417980.1:p.Lys895Met
ENST00000636027.1:c.2570A>T	ENSP00000489961.1:p.Lys857Met
ENST00000637161.1:c.2591A>T	ENSP00000490328.1:p.Lys864Met
ENST00000637261.1:c.2724A>T	ENSP00000490815.1:n.2724A>T
ENST00000637891.1:c.578A>T	ENSP00000490907.1:p.Lys193Met
ENST00000637949.1:c.362A>T	ENSP00000489786.1:p.Lys121Met
ENST00000460843.5:c.2684A>T	ENSP00000417980.1:p.Lys895Met
ENST00000462942.3:c.1541A>T	ENSP00000436107.1:p.Lys514Met
ENST00000482340.5:c.254A>T	ENSP00000486748.1:p.Lys85Met
ENST00000486164.5:c.262A>T
ENST00000488242.2:n.210A>T
ENST00000493484.5:c.254A>T	ENSP00000486503.1:p.Lys85Met
NM_024757.4:c.2684A>T	NP_079033.4:p.Lys895Met
XM_005266105.3:c.2675A>T	XP_005266162.1:p.Lys892Met
XM_005266110.1:c.2591A>T	XP_005266167.1:p.Lys864Met
XM_006717288.2:c.2666A>T	XP_006717351.1:p.Lys889Met
XM_011519021.1:c.2693A>T	XP_011517323.1:p.Lys898Met
XM_011519022.1:c.2690A>T	XP_011517324.1:p.Lys897Met
XM_011519023.1:c.2672A>T	XP_011517325.1:p.Lys891Met
XM_011519024.1:c.2615A>T	XP_011517326.1:p.Lys872Met
XM_011519025.1:c.2591A>T	XP_011517327.1:p.Lys864Met
XM_011519026.1:c.2549A>T	XP_011517328.1:p.Lys850Met
XM_011519027.1:c.2693A>T	XP_011517329.1:p.Lys898Met
XM_011519029.1:c.1115A>T	XP_011517331.1:p.Lys372Met
XM_011519030.1:c.467A>T	XP_011517332.1:p.Lys156Met
XM_011519031.1:c.254A>T	XP_011517333.1:p.Lys85Met
XM_011519032.1:c.254A>T	XP_011517334.1:p.Lys85Met
XM_011519033.1:c.2528A>T	XP_011517335.1:p.Lys843Met
NM_001354263.1:c.2663A>T	NP_001341192.1:p.Lys888Met
XM_005266105.5:c.2675A>T	XP_005266162.1:p.Lys892Met
XM_011519021.3:c.2693A>T	XP_011517323.1:p.Lys898Met
XM_011519022.3:c.2690A>T	XP_011517324.1:p.Lys897Met
XM_011519023.3:c.2672A>T	XP_011517325.1:p.Lys891Met
XM_011519029.3:c.1115A>T	XP_011517331.1:p.Lys372Met
XM_011519030.3:c.467A>T	XP_011517332.1:p.Lys156Met
XM_017015134.1:c.2669A>T	XP_016870623.1:p.Lys890Met
XM_017015136.2:c.2585A>T	XP_016870625.1:p.Lys862Met
XM_017015137.1:c.2570A>T	XP_016870626.1:p.Lys857Met
XM_017015138.1:c.2570A>T	XP_016870627.1:p.Lys857Met
XM_024447674.1:c.2513A>T	XP_024303442.1:p.Lys838Met
XM_024447675.1:c.2447A>T	XP_024303443.1:p.Lys816Met
XM_024447676.1:c.1808A>T	XP_024303444.1:p.Lys603Met
XM_024447677.1:c.1808A>T	XP_024303445.1:p.Lys603Met
XM_024447678.1:c.2591A>T	XP_024303446.1:p.Lys864Met
XM_024447680.1:c.2426A>T	XP_024303448.1:p.Lys809Met
NM_024757.5:c.2684A>T MANE Select	NP_079033.4:p.Lys895Met
NM_001354263.2:c.2663A>T	NP_001341192.1:p.Lys888Met