Canonical Allele Identifier: CA375793784

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707839G>C (hg19) ; chr9:g.137813387G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813387G>C , CM000671.2:g.137813387G>C	GRCh38
NC_000009.11:g.140707839G>C , CM000671.1:g.140707839G>C	GRCh37
NC_000009.10:g.139827660G>C	NCBI36
NG_011776.1:g.199396G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3037G>C MANE Select	ENSP00000417980.1:p.Asp1013His
ENST00000636027.1:c.2923G>C	ENSP00000489961.1:p.Asp975His
ENST00000637161.1:c.2944G>C	ENSP00000490328.1:p.Asp982His
ENST00000637261.1:c.3077G>C	ENSP00000490815.1:n.3077G>C
ENST00000637891.1:c.931G>C	ENSP00000490907.1:p.Asp311His
ENST00000460843.5:c.3037G>C	ENSP00000417980.1:p.Asp1013His
ENST00000462942.3:c.1894G>C	ENSP00000436107.1:p.Asp632His
ENST00000486164.5:c.724G>C
ENST00000488242.2:n.563G>C
NM_024757.4:c.3037G>C	NP_079033.4:p.Asp1013His
XM_005266105.3:c.3028G>C	XP_005266162.1:p.Asp1010His
XM_005266110.1:c.2944G>C	XP_005266167.1:p.Asp982His
XM_006717288.2:c.3019G>C	XP_006717351.1:p.Asp1007His
XM_011519021.1:c.3046G>C	XP_011517323.1:p.Asp1016His
XM_011519022.1:c.3043G>C	XP_011517324.1:p.Asp1015His
XM_011519023.1:c.3025G>C	XP_011517325.1:p.Asp1009His
XM_011519024.1:c.2968G>C	XP_011517326.1:p.Asp990His
XM_011519025.1:c.2944G>C	XP_011517327.1:p.Asp982His
XM_011519026.1:c.2902G>C	XP_011517328.1:p.Asp968His
XM_011519029.1:c.1468G>C	XP_011517331.1:p.Asp490His
XM_011519030.1:c.820G>C	XP_011517332.1:p.Asp274His
XM_011519031.1:c.607G>C	XP_011517333.1:p.Asp203His
XM_011519032.1:c.607G>C	XP_011517334.1:p.Asp203His
XM_011519033.1:c.2881G>C	XP_011517335.1:p.Asp961His
NM_001354263.1:c.3016G>C	NP_001341192.1:p.Asp1006His
XM_005266105.5:c.3028G>C	XP_005266162.1:p.Asp1010His
XM_011519021.3:c.3046G>C	XP_011517323.1:p.Asp1016His
XM_011519022.3:c.3043G>C	XP_011517324.1:p.Asp1015His
XM_011519023.3:c.3025G>C	XP_011517325.1:p.Asp1009His
XM_011519029.3:c.1468G>C	XP_011517331.1:p.Asp490His
XM_011519030.3:c.820G>C	XP_011517332.1:p.Asp274His
XM_017015134.1:c.3022G>C	XP_016870623.1:p.Asp1008His
XM_017015136.2:c.2938G>C	XP_016870625.1:p.Asp980His
XM_017015137.1:c.2923G>C	XP_016870626.1:p.Asp975His
XM_017015138.1:c.2923G>C	XP_016870627.1:p.Asp975His
XM_024447674.1:c.2866G>C	XP_024303442.1:p.Asp956His
XM_024447675.1:c.2800G>C	XP_024303443.1:p.Asp934His
XM_024447676.1:c.2161G>C	XP_024303444.1:p.Asp721His
XM_024447677.1:c.2161G>C	XP_024303445.1:p.Asp721His
XM_024447680.1:c.2779G>C	XP_024303448.1:p.Asp927His
NM_024757.5:c.3037G>C MANE Select	NP_079033.4:p.Asp1013His
NM_001354263.2:c.3016G>C	NP_001341192.1:p.Asp1006His