Canonical Allele Identifier: CA375773965

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712583A>C (hg19) ; chr9:g.137818131A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818131A>C , CM000671.2:g.137818131A>C	GRCh38
NC_000009.11:g.140712583A>C , CM000671.1:g.140712583A>C	GRCh37
NC_000009.10:g.139832404A>C	NCBI36
NG_011776.1:g.204140A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3533A>C MANE Select	ENSP00000417980.1:p.Asp1178Ala
ENST00000636472.1:n.95A>C
ENST00000636526.1:n.19A>C
ENST00000637161.1:c.3440A>C	ENSP00000490328.1:p.Asp1147Ala
ENST00000637261.1:c.4107A>C	ENSP00000490815.1:n.4107A>C
ENST00000637748.1:n.514A>C
ENST00000637891.1:c.1607A>C	ENSP00000490907.1:n.1607A>C
ENST00000460843.5:c.3533A>C	ENSP00000417980.1:p.Asp1178Ala
ENST00000462942.3:c.2390A>C	ENSP00000436107.1:p.Asp797Ala
ENST00000475564.5:n.1257A>C
ENST00000494249.5:n.886A>C
NM_024757.4:c.3533A>C	NP_079033.4:p.Asp1178Ala
XM_005266105.3:c.3524A>C	XP_005266162.1:p.Asp1175Ala
XM_005266110.1:c.3440A>C	XP_005266167.1:p.Asp1147Ala
XM_006717288.2:c.3515A>C	XP_006717351.1:p.Asp1172Ala
XM_011519021.1:c.3542A>C	XP_011517323.1:p.Asp1181Ala
XM_011519022.1:c.3539A>C	XP_011517324.1:p.Asp1180Ala
XM_011519023.1:c.3521A>C	XP_011517325.1:p.Asp1174Ala
XM_011519024.1:c.3464A>C	XP_011517326.1:p.Asp1155Ala
XM_011519025.1:c.3440A>C	XP_011517327.1:p.Asp1147Ala
XM_011519026.1:c.3398A>C	XP_011517328.1:p.Asp1133Ala
XM_011519029.1:c.1964A>C	XP_011517331.1:p.Asp655Ala
XM_011519030.1:c.1316A>C	XP_011517332.1:p.Asp439Ala
XM_011519031.1:c.1103A>C	XP_011517333.1:p.Asp368Ala
XM_011519032.1:c.1103A>C	XP_011517334.1:p.Asp368Ala
XM_011519033.1:c.3377A>C	XP_011517335.1:p.Asp1126Ala
XR_930459.1:n.5297-3569T>G
NM_001354263.1:c.3512A>C	NP_001341192.1:p.Asp1171Ala
XM_005266105.5:c.3524A>C	XP_005266162.1:p.Asp1175Ala
XM_011519021.3:c.3542A>C	XP_011517323.1:p.Asp1181Ala
XM_011519022.3:c.3539A>C	XP_011517324.1:p.Asp1180Ala
XM_011519023.3:c.3521A>C	XP_011517325.1:p.Asp1174Ala
XM_011519029.3:c.1964A>C	XP_011517331.1:p.Asp655Ala
XM_011519030.3:c.1316A>C	XP_011517332.1:p.Asp439Ala
XM_017015134.1:c.3518A>C	XP_016870623.1:p.Asp1173Ala
XM_017015136.2:c.3434A>C	XP_016870625.1:p.Asp1145Ala
XM_017015137.1:c.3419A>C	XP_016870626.1:p.Asp1140Ala
XM_017015138.1:c.3419A>C	XP_016870627.1:p.Asp1140Ala
XM_024447674.1:c.3362A>C	XP_024303442.1:p.Asp1121Ala
XM_024447675.1:c.3296A>C	XP_024303443.1:p.Asp1099Ala
XM_024447676.1:c.2657A>C	XP_024303444.1:p.Asp886Ala
XM_024447677.1:c.2657A>C	XP_024303445.1:p.Asp886Ala
XM_024447680.1:c.3275A>C	XP_024303448.1:p.Asp1092Ala
NM_024757.5:c.3533A>C MANE Select	NP_079033.4:p.Asp1178Ala
NM_001354263.2:c.3512A>C	NP_001341192.1:p.Asp1171Ala