Canonical Allele Identifier: CA375776620

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671212C>G (hg19) ; chr9:g.137776760C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776760C>G , CM000671.2:g.137776760C>G	GRCh38
NC_000009.11:g.140671212C>G , CM000671.1:g.140671212C>G	GRCh37
NC_000009.10:g.139791033C>G	NCBI36
NG_011776.1:g.162769C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1934C>G MANE Select	ENSP00000417980.1:p.Ala645Gly
ENST00000636027.1:c.1820C>G	ENSP00000489961.1:p.Ala607Gly
ENST00000637161.1:c.1841C>G	ENSP00000490328.1:p.Ala614Gly
ENST00000637261.1:c.1974C>G	ENSP00000490815.1:n.1974C>G
ENST00000638071.1:c.1561C>G
ENST00000640639.1:c.1103C>G	ENSP00000491823.1:p.Ala368Gly
ENST00000371394.6:c.*1669C>G	ENSP00000485945.1:n.*1669C>G
ENST00000460843.5:c.1934C>G	ENSP00000417980.1:p.Ala645Gly
ENST00000462484.5:c.1934C>G	ENSP00000417328.1:p.Ala645Gly
ENST00000462942.3:c.791C>G	ENSP00000436107.1:p.Ala264Gly
ENST00000465566.2:c.482C>G	ENSP00000486261.1:p.Ala161Gly
ENST00000626603.1:n.1689G>C
NM_001145527.1:c.1934C>G	NP_001138999.1:p.Ala645Gly
NM_024757.4:c.1934C>G	NP_079033.4:p.Ala645Gly
XM_005266105.3:c.1925C>G	XP_005266162.1:p.Ala642Gly
XM_005266110.1:c.1841C>G	XP_005266167.1:p.Ala614Gly
XM_006717288.2:c.1916C>G	XP_006717351.1:p.Ala639Gly
XM_011519021.1:c.1943C>G	XP_011517323.1:p.Ala648Gly
XM_011519022.1:c.1940C>G	XP_011517324.1:p.Ala647Gly
XM_011519023.1:c.1922C>G	XP_011517325.1:p.Ala641Gly
XM_011519024.1:c.1865C>G	XP_011517326.1:p.Ala622Gly
XM_011519025.1:c.1841C>G	XP_011517327.1:p.Ala614Gly
XM_011519026.1:c.1799C>G	XP_011517328.1:p.Ala600Gly
XM_011519027.1:c.1943C>G	XP_011517329.1:p.Ala648Gly
XM_011519028.1:c.1943C>G	XP_011517330.1:p.Ala648Gly
XM_011519029.1:c.365C>G	XP_011517331.1:p.Ala122Gly
XM_011519033.1:c.1778C>G	XP_011517335.1:p.Ala593Gly
NM_001354259.1:c.1841C>G	NP_001341188.1:p.Ala614Gly
NM_001354263.1:c.1913C>G	NP_001341192.1:p.Ala638Gly
XM_005266105.5:c.1925C>G	XP_005266162.1:p.Ala642Gly
XM_011519021.3:c.1943C>G	XP_011517323.1:p.Ala648Gly
XM_011519022.3:c.1940C>G	XP_011517324.1:p.Ala647Gly
XM_011519023.3:c.1922C>G	XP_011517325.1:p.Ala641Gly
XM_011519029.3:c.365C>G	XP_011517331.1:p.Ala122Gly
XM_017015134.1:c.1919C>G	XP_016870623.1:p.Ala640Gly
XM_017015136.2:c.1835C>G	XP_016870625.1:p.Ala612Gly
XM_017015137.1:c.1820C>G	XP_016870626.1:p.Ala607Gly
XM_017015138.1:c.1820C>G	XP_016870627.1:p.Ala607Gly
XM_024447674.1:c.1763C>G	XP_024303442.1:p.Ala588Gly
XM_024447675.1:c.1697C>G	XP_024303443.1:p.Ala566Gly
XM_024447676.1:c.1058C>G	XP_024303444.1:p.Ala353Gly
XM_024447677.1:c.1058C>G	XP_024303445.1:p.Ala353Gly
XM_024447678.1:c.1841C>G	XP_024303446.1:p.Ala614Gly
XM_024447679.1:c.1841C>G	XP_024303447.1:p.Ala614Gly
XM_024447680.1:c.1676C>G	XP_024303448.1:p.Ala559Gly
NM_024757.5:c.1934C>G MANE Select	NP_079033.4:p.Ala645Gly
NM_001145527.2:c.1934C>G	NP_001138999.1:p.Ala645Gly
NM_001354259.2:c.1841C>G	NP_001341188.1:p.Ala614Gly
NM_001354263.2:c.1913C>G	NP_001341192.1:p.Ala638Gly