Canonical Allele Identifier: CA375793318

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707496A>C (hg19) ; chr9:g.137813044A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813044A>C , CM000671.2:g.137813044A>C	GRCh38
NC_000009.11:g.140707496A>C , CM000671.1:g.140707496A>C	GRCh37
NC_000009.10:g.139827317A>C	NCBI36
NG_011776.1:g.199053A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2906A>C MANE Select	ENSP00000417980.1:p.Asn969Thr
ENST00000636027.1:c.2792A>C	ENSP00000489961.1:p.Asn931Thr
ENST00000637161.1:c.2813A>C	ENSP00000490328.1:p.Asn938Thr
ENST00000637261.1:c.2946A>C	ENSP00000490815.1:n.2946A>C
ENST00000637891.1:c.800A>C	ENSP00000490907.1:p.Asn267Thr
ENST00000460843.5:c.2906A>C	ENSP00000417980.1:p.Asn969Thr
ENST00000462942.3:c.1763A>C	ENSP00000436107.1:p.Asn588Thr
ENST00000486164.5:c.593A>C
ENST00000488242.2:n.432A>C
NM_024757.4:c.2906A>C	NP_079033.4:p.Asn969Thr
XM_005266105.3:c.2897A>C	XP_005266162.1:p.Asn966Thr
XM_005266110.1:c.2813A>C	XP_005266167.1:p.Asn938Thr
XM_006717288.2:c.2888A>C	XP_006717351.1:p.Asn963Thr
XM_011519021.1:c.2915A>C	XP_011517323.1:p.Asn972Thr
XM_011519022.1:c.2912A>C	XP_011517324.1:p.Asn971Thr
XM_011519023.1:c.2894A>C	XP_011517325.1:p.Asn965Thr
XM_011519024.1:c.2837A>C	XP_011517326.1:p.Asn946Thr
XM_011519025.1:c.2813A>C	XP_011517327.1:p.Asn938Thr
XM_011519026.1:c.2771A>C	XP_011517328.1:p.Asn924Thr
XM_011519029.1:c.1337A>C	XP_011517331.1:p.Asn446Thr
XM_011519030.1:c.689A>C	XP_011517332.1:p.Asn230Thr
XM_011519031.1:c.476A>C	XP_011517333.1:p.Asn159Thr
XM_011519032.1:c.476A>C	XP_011517334.1:p.Asn159Thr
XM_011519033.1:c.2750A>C	XP_011517335.1:p.Asn917Thr
NM_001354263.1:c.2885A>C	NP_001341192.1:p.Asn962Thr
XM_005266105.5:c.2897A>C	XP_005266162.1:p.Asn966Thr
XM_011519021.3:c.2915A>C	XP_011517323.1:p.Asn972Thr
XM_011519022.3:c.2912A>C	XP_011517324.1:p.Asn971Thr
XM_011519023.3:c.2894A>C	XP_011517325.1:p.Asn965Thr
XM_011519029.3:c.1337A>C	XP_011517331.1:p.Asn446Thr
XM_011519030.3:c.689A>C	XP_011517332.1:p.Asn230Thr
XM_017015134.1:c.2891A>C	XP_016870623.1:p.Asn964Thr
XM_017015136.2:c.2807A>C	XP_016870625.1:p.Asn936Thr
XM_017015137.1:c.2792A>C	XP_016870626.1:p.Asn931Thr
XM_017015138.1:c.2792A>C	XP_016870627.1:p.Asn931Thr
XM_024447674.1:c.2735A>C	XP_024303442.1:p.Asn912Thr
XM_024447675.1:c.2669A>C	XP_024303443.1:p.Asn890Thr
XM_024447676.1:c.2030A>C	XP_024303444.1:p.Asn677Thr
XM_024447677.1:c.2030A>C	XP_024303445.1:p.Asn677Thr
XM_024447680.1:c.2648A>C	XP_024303448.1:p.Asn883Thr
NM_024757.5:c.2906A>C MANE Select	NP_079033.4:p.Asn969Thr
NM_001354263.2:c.2885A>C	NP_001341192.1:p.Asn962Thr