Canonical Allele Identifier: CA375788865

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695376G>C (hg19) ; chr9:g.137800924G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800924G>C , CM000671.2:g.137800924G>C	GRCh38
NC_000009.11:g.140695376G>C , CM000671.1:g.140695376G>C	GRCh37
NC_000009.10:g.139815197G>C	NCBI36
NG_011776.1:g.186933G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2652G>C MANE Select	ENSP00000417980.1:p.Lys884Asn
ENST00000636027.1:c.2538G>C	ENSP00000489961.1:p.Lys846Asn
ENST00000637161.1:c.2559G>C	ENSP00000490328.1:p.Lys853Asn
ENST00000637261.1:c.2692G>C	ENSP00000490815.1:n.2692G>C
ENST00000637891.1:c.546G>C	ENSP00000490907.1:p.Lys182Asn
ENST00000637949.1:c.330G>C	ENSP00000489786.1:p.Lys110Asn
ENST00000460843.5:c.2652G>C	ENSP00000417980.1:p.Lys884Asn
ENST00000462942.3:c.1509G>C	ENSP00000436107.1:p.Lys503Asn
ENST00000482340.5:c.222G>C	ENSP00000486748.1:p.Lys74Asn
ENST00000486164.5:c.230G>C
ENST00000488242.2:n.178G>C
ENST00000493484.5:c.222G>C	ENSP00000486503.1:p.Lys74Asn
NM_024757.4:c.2652G>C	NP_079033.4:p.Lys884Asn
XM_005266105.3:c.2643G>C	XP_005266162.1:p.Lys881Asn
XM_005266110.1:c.2559G>C	XP_005266167.1:p.Lys853Asn
XM_006717288.2:c.2634G>C	XP_006717351.1:p.Lys878Asn
XM_011519021.1:c.2661G>C	XP_011517323.1:p.Lys887Asn
XM_011519022.1:c.2658G>C	XP_011517324.1:p.Lys886Asn
XM_011519023.1:c.2640G>C	XP_011517325.1:p.Lys880Asn
XM_011519024.1:c.2583G>C	XP_011517326.1:p.Lys861Asn
XM_011519025.1:c.2559G>C	XP_011517327.1:p.Lys853Asn
XM_011519026.1:c.2517G>C	XP_011517328.1:p.Lys839Asn
XM_011519027.1:c.2661G>C	XP_011517329.1:p.Lys887Asn
XM_011519029.1:c.1083G>C	XP_011517331.1:p.Lys361Asn
XM_011519030.1:c.435G>C	XP_011517332.1:p.Lys145Asn
XM_011519031.1:c.222G>C	XP_011517333.1:p.Lys74Asn
XM_011519032.1:c.222G>C	XP_011517334.1:p.Lys74Asn
XM_011519033.1:c.2496G>C	XP_011517335.1:p.Lys832Asn
NM_001354263.1:c.2631G>C	NP_001341192.1:p.Lys877Asn
XM_005266105.5:c.2643G>C	XP_005266162.1:p.Lys881Asn
XM_011519021.3:c.2661G>C	XP_011517323.1:p.Lys887Asn
XM_011519022.3:c.2658G>C	XP_011517324.1:p.Lys886Asn
XM_011519023.3:c.2640G>C	XP_011517325.1:p.Lys880Asn
XM_011519029.3:c.1083G>C	XP_011517331.1:p.Lys361Asn
XM_011519030.3:c.435G>C	XP_011517332.1:p.Lys145Asn
XM_017015134.1:c.2637G>C	XP_016870623.1:p.Lys879Asn
XM_017015136.2:c.2553G>C	XP_016870625.1:p.Lys851Asn
XM_017015137.1:c.2538G>C	XP_016870626.1:p.Lys846Asn
XM_017015138.1:c.2538G>C	XP_016870627.1:p.Lys846Asn
XM_024447674.1:c.2481G>C	XP_024303442.1:p.Lys827Asn
XM_024447675.1:c.2415G>C	XP_024303443.1:p.Lys805Asn
XM_024447676.1:c.1776G>C	XP_024303444.1:p.Lys592Asn
XM_024447677.1:c.1776G>C	XP_024303445.1:p.Lys592Asn
XM_024447678.1:c.2559G>C	XP_024303446.1:p.Lys853Asn
XM_024447680.1:c.2394G>C	XP_024303448.1:p.Lys798Asn
NM_024757.5:c.2652G>C MANE Select	NP_079033.4:p.Lys884Asn
NM_001354263.2:c.2631G>C	NP_001341192.1:p.Lys877Asn