Canonical Allele Identifier: CA375776647

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671215A>G (hg19) ; chr9:g.137776763A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776763A>G , CM000671.2:g.137776763A>G	GRCh38
NC_000009.11:g.140671215A>G , CM000671.1:g.140671215A>G	GRCh37
NC_000009.10:g.139791036A>G	NCBI36
NG_011776.1:g.162772A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1937A>G MANE Select	ENSP00000417980.1:p.Asp646Gly
ENST00000636027.1:c.1823A>G	ENSP00000489961.1:p.Asp608Gly
ENST00000637161.1:c.1844A>G	ENSP00000490328.1:p.Asp615Gly
ENST00000637261.1:c.1977A>G	ENSP00000490815.1:n.1977A>G
ENST00000638071.1:c.1564A>G
ENST00000640639.1:c.1106A>G	ENSP00000491823.1:p.Asp369Gly
ENST00000371394.6:c.*1672A>G	ENSP00000485945.1:n.*1672A>G
ENST00000460843.5:c.1937A>G	ENSP00000417980.1:p.Asp646Gly
ENST00000462484.5:c.1937A>G	ENSP00000417328.1:p.Asp646Gly
ENST00000462942.3:c.794A>G	ENSP00000436107.1:p.Asp265Gly
ENST00000465566.2:c.485A>G	ENSP00000486261.1:p.Asp162Gly
ENST00000626603.1:n.1686T>C
NM_001145527.1:c.1937A>G	NP_001138999.1:p.Asp646Gly
NM_024757.4:c.1937A>G	NP_079033.4:p.Asp646Gly
XM_005266105.3:c.1928A>G	XP_005266162.1:p.Asp643Gly
XM_005266110.1:c.1844A>G	XP_005266167.1:p.Asp615Gly
XM_006717288.2:c.1919A>G	XP_006717351.1:p.Asp640Gly
XM_011519021.1:c.1946A>G	XP_011517323.1:p.Asp649Gly
XM_011519022.1:c.1943A>G	XP_011517324.1:p.Asp648Gly
XM_011519023.1:c.1925A>G	XP_011517325.1:p.Asp642Gly
XM_011519024.1:c.1868A>G	XP_011517326.1:p.Asp623Gly
XM_011519025.1:c.1844A>G	XP_011517327.1:p.Asp615Gly
XM_011519026.1:c.1802A>G	XP_011517328.1:p.Asp601Gly
XM_011519027.1:c.1946A>G	XP_011517329.1:p.Asp649Gly
XM_011519028.1:c.1946A>G	XP_011517330.1:p.Asp649Gly
XM_011519029.1:c.368A>G	XP_011517331.1:p.Asp123Gly
XM_011519033.1:c.1781A>G	XP_011517335.1:p.Asp594Gly
NM_001354259.1:c.1844A>G	NP_001341188.1:p.Asp615Gly
NM_001354263.1:c.1916A>G	NP_001341192.1:p.Asp639Gly
XM_005266105.5:c.1928A>G	XP_005266162.1:p.Asp643Gly
XM_011519021.3:c.1946A>G	XP_011517323.1:p.Asp649Gly
XM_011519022.3:c.1943A>G	XP_011517324.1:p.Asp648Gly
XM_011519023.3:c.1925A>G	XP_011517325.1:p.Asp642Gly
XM_011519029.3:c.368A>G	XP_011517331.1:p.Asp123Gly
XM_017015134.1:c.1922A>G	XP_016870623.1:p.Asp641Gly
XM_017015136.2:c.1838A>G	XP_016870625.1:p.Asp613Gly
XM_017015137.1:c.1823A>G	XP_016870626.1:p.Asp608Gly
XM_017015138.1:c.1823A>G	XP_016870627.1:p.Asp608Gly
XM_024447674.1:c.1766A>G	XP_024303442.1:p.Asp589Gly
XM_024447675.1:c.1700A>G	XP_024303443.1:p.Asp567Gly
XM_024447676.1:c.1061A>G	XP_024303444.1:p.Asp354Gly
XM_024447677.1:c.1061A>G	XP_024303445.1:p.Asp354Gly
XM_024447678.1:c.1844A>G	XP_024303446.1:p.Asp615Gly
XM_024447679.1:c.1844A>G	XP_024303447.1:p.Asp615Gly
XM_024447680.1:c.1679A>G	XP_024303448.1:p.Asp560Gly
NM_024757.5:c.1937A>G MANE Select	NP_079033.4:p.Asp646Gly
NM_001145527.2:c.1937A>G	NP_001138999.1:p.Asp646Gly
NM_001354259.2:c.1844A>G	NP_001341188.1:p.Asp615Gly
NM_001354263.2:c.1916A>G	NP_001341192.1:p.Asp639Gly