Canonical Allele Identifier: CA375776625

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671214G>T (hg19) ; chr9:g.137776762G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776762G>T , CM000671.2:g.137776762G>T	GRCh38
NC_000009.11:g.140671214G>T , CM000671.1:g.140671214G>T	GRCh37
NC_000009.10:g.139791035G>T	NCBI36
NG_011776.1:g.162771G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1936G>T MANE Select	ENSP00000417980.1:p.Asp646Tyr
ENST00000636027.1:c.1822G>T	ENSP00000489961.1:p.Asp608Tyr
ENST00000637161.1:c.1843G>T	ENSP00000490328.1:p.Asp615Tyr
ENST00000637261.1:c.1976G>T	ENSP00000490815.1:n.1976G>T
ENST00000638071.1:c.1563G>T
ENST00000640639.1:c.1105G>T	ENSP00000491823.1:p.Asp369Tyr
ENST00000371394.6:c.*1671G>T	ENSP00000485945.1:n.*1671G>T
ENST00000460843.5:c.1936G>T	ENSP00000417980.1:p.Asp646Tyr
ENST00000462484.5:c.1936G>T	ENSP00000417328.1:p.Asp646Tyr
ENST00000462942.3:c.793G>T	ENSP00000436107.1:p.Asp265Tyr
ENST00000465566.2:c.484G>T	ENSP00000486261.1:p.Asp162Tyr
ENST00000626603.1:n.1687C>A
NM_001145527.1:c.1936G>T	NP_001138999.1:p.Asp646Tyr
NM_024757.4:c.1936G>T	NP_079033.4:p.Asp646Tyr
XM_005266105.3:c.1927G>T	XP_005266162.1:p.Asp643Tyr
XM_005266110.1:c.1843G>T	XP_005266167.1:p.Asp615Tyr
XM_006717288.2:c.1918G>T	XP_006717351.1:p.Asp640Tyr
XM_011519021.1:c.1945G>T	XP_011517323.1:p.Asp649Tyr
XM_011519022.1:c.1942G>T	XP_011517324.1:p.Asp648Tyr
XM_011519023.1:c.1924G>T	XP_011517325.1:p.Asp642Tyr
XM_011519024.1:c.1867G>T	XP_011517326.1:p.Asp623Tyr
XM_011519025.1:c.1843G>T	XP_011517327.1:p.Asp615Tyr
XM_011519026.1:c.1801G>T	XP_011517328.1:p.Asp601Tyr
XM_011519027.1:c.1945G>T	XP_011517329.1:p.Asp649Tyr
XM_011519028.1:c.1945G>T	XP_011517330.1:p.Asp649Tyr
XM_011519029.1:c.367G>T	XP_011517331.1:p.Asp123Tyr
XM_011519033.1:c.1780G>T	XP_011517335.1:p.Asp594Tyr
NM_001354259.1:c.1843G>T	NP_001341188.1:p.Asp615Tyr
NM_001354263.1:c.1915G>T	NP_001341192.1:p.Asp639Tyr
XM_005266105.5:c.1927G>T	XP_005266162.1:p.Asp643Tyr
XM_011519021.3:c.1945G>T	XP_011517323.1:p.Asp649Tyr
XM_011519022.3:c.1942G>T	XP_011517324.1:p.Asp648Tyr
XM_011519023.3:c.1924G>T	XP_011517325.1:p.Asp642Tyr
XM_011519029.3:c.367G>T	XP_011517331.1:p.Asp123Tyr
XM_017015134.1:c.1921G>T	XP_016870623.1:p.Asp641Tyr
XM_017015136.2:c.1837G>T	XP_016870625.1:p.Asp613Tyr
XM_017015137.1:c.1822G>T	XP_016870626.1:p.Asp608Tyr
XM_017015138.1:c.1822G>T	XP_016870627.1:p.Asp608Tyr
XM_024447674.1:c.1765G>T	XP_024303442.1:p.Asp589Tyr
XM_024447675.1:c.1699G>T	XP_024303443.1:p.Asp567Tyr
XM_024447676.1:c.1060G>T	XP_024303444.1:p.Asp354Tyr
XM_024447677.1:c.1060G>T	XP_024303445.1:p.Asp354Tyr
XM_024447678.1:c.1843G>T	XP_024303446.1:p.Asp615Tyr
XM_024447679.1:c.1843G>T	XP_024303447.1:p.Asp615Tyr
XM_024447680.1:c.1678G>T	XP_024303448.1:p.Asp560Tyr
NM_024757.5:c.1936G>T MANE Select	NP_079033.4:p.Asp646Tyr
NM_001145527.2:c.1936G>T	NP_001138999.1:p.Asp646Tyr
NM_001354259.2:c.1843G>T	NP_001341188.1:p.Asp615Tyr
NM_001354263.2:c.1915G>T	NP_001341192.1:p.Asp639Tyr