Canonical Allele Identifier: CA375794566

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707966A>C (hg19) ; chr9:g.137813514A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813514A>C , CM000671.2:g.137813514A>C	GRCh38
NC_000009.11:g.140707966A>C , CM000671.1:g.140707966A>C	GRCh37
NC_000009.10:g.139827787A>C	NCBI36
NG_011776.1:g.199523A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3164A>C MANE Select	ENSP00000417980.1:p.Asn1055Thr
ENST00000637161.1:c.3071A>C	ENSP00000490328.1:p.Asn1024Thr
ENST00000637261.1:c.3204A>C	ENSP00000490815.1:n.3204A>C
ENST00000637891.1:c.1058A>C	ENSP00000490907.1:p.Asn353Thr
ENST00000460843.5:c.3164A>C	ENSP00000417980.1:p.Asn1055Thr
ENST00000462942.3:c.2021A>C	ENSP00000436107.1:p.Asn674Thr
ENST00000483653.1:n.24A>C
ENST00000488242.2:n.690A>C
NM_024757.4:c.3164A>C	NP_079033.4:p.Asn1055Thr
XM_005266105.3:c.3155A>C	XP_005266162.1:p.Asn1052Thr
XM_005266110.1:c.3071A>C	XP_005266167.1:p.Asn1024Thr
XM_006717288.2:c.3146A>C	XP_006717351.1:p.Asn1049Thr
XM_011519021.1:c.3173A>C	XP_011517323.1:p.Asn1058Thr
XM_011519022.1:c.3170A>C	XP_011517324.1:p.Asn1057Thr
XM_011519023.1:c.3152A>C	XP_011517325.1:p.Asn1051Thr
XM_011519024.1:c.3095A>C	XP_011517326.1:p.Asn1032Thr
XM_011519025.1:c.3071A>C	XP_011517327.1:p.Asn1024Thr
XM_011519026.1:c.3029A>C	XP_011517328.1:p.Asn1010Thr
XM_011519029.1:c.1595A>C	XP_011517331.1:p.Asn532Thr
XM_011519030.1:c.947A>C	XP_011517332.1:p.Asn316Thr
XM_011519031.1:c.734A>C	XP_011517333.1:p.Asn245Thr
XM_011519032.1:c.734A>C	XP_011517334.1:p.Asn245Thr
XM_011519033.1:c.3008A>C	XP_011517335.1:p.Asn1003Thr
NM_001354263.1:c.3143A>C	NP_001341192.1:p.Asn1048Thr
XM_005266105.5:c.3155A>C	XP_005266162.1:p.Asn1052Thr
XM_011519021.3:c.3173A>C	XP_011517323.1:p.Asn1058Thr
XM_011519022.3:c.3170A>C	XP_011517324.1:p.Asn1057Thr
XM_011519023.3:c.3152A>C	XP_011517325.1:p.Asn1051Thr
XM_011519029.3:c.1595A>C	XP_011517331.1:p.Asn532Thr
XM_011519030.3:c.947A>C	XP_011517332.1:p.Asn316Thr
XM_017015134.1:c.3149A>C	XP_016870623.1:p.Asn1050Thr
XM_017015136.2:c.3065A>C	XP_016870625.1:p.Asn1022Thr
XM_017015137.1:c.3050A>C	XP_016870626.1:p.Asn1017Thr
XM_017015138.1:c.3050A>C	XP_016870627.1:p.Asn1017Thr
XM_024447674.1:c.2993A>C	XP_024303442.1:p.Asn998Thr
XM_024447675.1:c.2927A>C	XP_024303443.1:p.Asn976Thr
XM_024447676.1:c.2288A>C	XP_024303444.1:p.Asn763Thr
XM_024447677.1:c.2288A>C	XP_024303445.1:p.Asn763Thr
XM_024447680.1:c.2906A>C	XP_024303448.1:p.Asn969Thr
NM_024757.5:c.3164A>C MANE Select	NP_079033.4:p.Asn1055Thr
NM_001354263.2:c.3143A>C	NP_001341192.1:p.Asn1048Thr