Canonical Allele Identifier: CA375789001

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695414C>T (hg19) ; chr9:g.137800962C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800962C>T , CM000671.2:g.137800962C>T	GRCh38
NC_000009.11:g.140695414C>T , CM000671.1:g.140695414C>T	GRCh37
NC_000009.10:g.139815235C>T	NCBI36
NG_011776.1:g.186971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2690C>T MANE Select	ENSP00000417980.1:p.Ser897Phe
ENST00000636027.1:c.2576C>T	ENSP00000489961.1:p.Ser859Phe
ENST00000637161.1:c.2597C>T	ENSP00000490328.1:p.Ser866Phe
ENST00000637261.1:c.2730C>T	ENSP00000490815.1:n.2730C>T
ENST00000637891.1:c.584C>T	ENSP00000490907.1:p.Ser195Phe
ENST00000637949.1:c.368C>T	ENSP00000489786.1:p.Ser123Phe
ENST00000460843.5:c.2690C>T	ENSP00000417980.1:p.Ser897Phe
ENST00000462942.3:c.1547C>T	ENSP00000436107.1:p.Ser516Phe
ENST00000482340.5:c.260C>T	ENSP00000486748.1:p.Ser87Phe
ENST00000486164.5:c.268C>T
ENST00000488242.2:n.216C>T
ENST00000493484.5:c.260C>T	ENSP00000486503.1:p.Ser87Phe
NM_024757.4:c.2690C>T	NP_079033.4:p.Ser897Phe
XM_005266105.3:c.2681C>T	XP_005266162.1:p.Ser894Phe
XM_005266110.1:c.2597C>T	XP_005266167.1:p.Ser866Phe
XM_006717288.2:c.2672C>T	XP_006717351.1:p.Ser891Phe
XM_011519021.1:c.2699C>T	XP_011517323.1:p.Ser900Phe
XM_011519022.1:c.2696C>T	XP_011517324.1:p.Ser899Phe
XM_011519023.1:c.2678C>T	XP_011517325.1:p.Ser893Phe
XM_011519024.1:c.2621C>T	XP_011517326.1:p.Ser874Phe
XM_011519025.1:c.2597C>T	XP_011517327.1:p.Ser866Phe
XM_011519026.1:c.2555C>T	XP_011517328.1:p.Ser852Phe
XM_011519027.1:c.2699C>T	XP_011517329.1:p.Ser900Phe
XM_011519029.1:c.1121C>T	XP_011517331.1:p.Ser374Phe
XM_011519030.1:c.473C>T	XP_011517332.1:p.Ser158Phe
XM_011519031.1:c.260C>T	XP_011517333.1:p.Ser87Phe
XM_011519032.1:c.260C>T	XP_011517334.1:p.Ser87Phe
XM_011519033.1:c.2534C>T	XP_011517335.1:p.Ser845Phe
NM_001354263.1:c.2669C>T	NP_001341192.1:p.Ser890Phe
XM_005266105.5:c.2681C>T	XP_005266162.1:p.Ser894Phe
XM_011519021.3:c.2699C>T	XP_011517323.1:p.Ser900Phe
XM_011519022.3:c.2696C>T	XP_011517324.1:p.Ser899Phe
XM_011519023.3:c.2678C>T	XP_011517325.1:p.Ser893Phe
XM_011519029.3:c.1121C>T	XP_011517331.1:p.Ser374Phe
XM_011519030.3:c.473C>T	XP_011517332.1:p.Ser158Phe
XM_017015134.1:c.2675C>T	XP_016870623.1:p.Ser892Phe
XM_017015136.2:c.2591C>T	XP_016870625.1:p.Ser864Phe
XM_017015137.1:c.2576C>T	XP_016870626.1:p.Ser859Phe
XM_017015138.1:c.2576C>T	XP_016870627.1:p.Ser859Phe
XM_024447674.1:c.2519C>T	XP_024303442.1:p.Ser840Phe
XM_024447675.1:c.2453C>T	XP_024303443.1:p.Ser818Phe
XM_024447676.1:c.1814C>T	XP_024303444.1:p.Ser605Phe
XM_024447677.1:c.1814C>T	XP_024303445.1:p.Ser605Phe
XM_024447678.1:c.2597C>T	XP_024303446.1:p.Ser866Phe
XM_024447680.1:c.2432C>T	XP_024303448.1:p.Ser811Phe
NM_024757.5:c.2690C>T MANE Select	NP_079033.4:p.Ser897Phe
NM_001354263.2:c.2669C>T	NP_001341192.1:p.Ser890Phe