Canonical Allele Identifier: CA375776779

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671238G>T (hg19) ; chr9:g.137776786G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776786G>T , CM000671.2:g.137776786G>T	GRCh38
NC_000009.11:g.140671238G>T , CM000671.1:g.140671238G>T	GRCh37
NC_000009.10:g.139791059G>T	NCBI36
NG_011776.1:g.162795G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1960G>T MANE Select	ENSP00000417980.1:p.Val654Phe
ENST00000636027.1:c.1846G>T	ENSP00000489961.1:p.Val616Phe
ENST00000637161.1:c.1867G>T	ENSP00000490328.1:p.Val623Phe
ENST00000637261.1:c.2000G>T	ENSP00000490815.1:n.2000G>T
ENST00000638071.1:c.1587G>T
ENST00000640639.1:c.1129G>T	ENSP00000491823.1:p.Val377Phe
ENST00000371394.6:c.*1695G>T	ENSP00000485945.1:n.*1695G>T
ENST00000460843.5:c.1960G>T	ENSP00000417980.1:p.Val654Phe
ENST00000462484.5:c.1960G>T	ENSP00000417328.1:p.Val654Phe
ENST00000462942.3:c.817G>T	ENSP00000436107.1:p.Val273Phe
ENST00000626603.1:n.1663C>A
NM_001145527.1:c.1960G>T	NP_001138999.1:p.Val654Phe
NM_024757.4:c.1960G>T	NP_079033.4:p.Val654Phe
XM_005266105.3:c.1951G>T	XP_005266162.1:p.Val651Phe
XM_005266110.1:c.1867G>T	XP_005266167.1:p.Val623Phe
XM_006717288.2:c.1942G>T	XP_006717351.1:p.Val648Phe
XM_011519021.1:c.1969G>T	XP_011517323.1:p.Val657Phe
XM_011519022.1:c.1966G>T	XP_011517324.1:p.Val656Phe
XM_011519023.1:c.1948G>T	XP_011517325.1:p.Val650Phe
XM_011519024.1:c.1891G>T	XP_011517326.1:p.Val631Phe
XM_011519025.1:c.1867G>T	XP_011517327.1:p.Val623Phe
XM_011519026.1:c.1825G>T	XP_011517328.1:p.Val609Phe
XM_011519027.1:c.1969G>T	XP_011517329.1:p.Val657Phe
XM_011519028.1:c.1969G>T	XP_011517330.1:p.Val657Phe
XM_011519029.1:c.391G>T	XP_011517331.1:p.Val131Phe
XM_011519033.1:c.1804G>T	XP_011517335.1:p.Val602Phe
NM_001354259.1:c.1867G>T	NP_001341188.1:p.Val623Phe
NM_001354263.1:c.1939G>T	NP_001341192.1:p.Val647Phe
XM_005266105.5:c.1951G>T	XP_005266162.1:p.Val651Phe
XM_011519021.3:c.1969G>T	XP_011517323.1:p.Val657Phe
XM_011519022.3:c.1966G>T	XP_011517324.1:p.Val656Phe
XM_011519023.3:c.1948G>T	XP_011517325.1:p.Val650Phe
XM_011519029.3:c.391G>T	XP_011517331.1:p.Val131Phe
XM_017015134.1:c.1945G>T	XP_016870623.1:p.Val649Phe
XM_017015136.2:c.1861G>T	XP_016870625.1:p.Val621Phe
XM_017015137.1:c.1846G>T	XP_016870626.1:p.Val616Phe
XM_017015138.1:c.1846G>T	XP_016870627.1:p.Val616Phe
XM_024447674.1:c.1789G>T	XP_024303442.1:p.Val597Phe
XM_024447675.1:c.1723G>T	XP_024303443.1:p.Val575Phe
XM_024447676.1:c.1084G>T	XP_024303444.1:p.Val362Phe
XM_024447677.1:c.1084G>T	XP_024303445.1:p.Val362Phe
XM_024447678.1:c.1867G>T	XP_024303446.1:p.Val623Phe
XM_024447679.1:c.1867G>T	XP_024303447.1:p.Val623Phe
XM_024447680.1:c.1702G>T	XP_024303448.1:p.Val568Phe
NM_024757.5:c.1960G>T MANE Select	NP_079033.4:p.Val654Phe
NM_001145527.2:c.1960G>T	NP_001138999.1:p.Val654Phe
NM_001354259.2:c.1867G>T	NP_001341188.1:p.Val623Phe
NM_001354263.2:c.1939G>T	NP_001341192.1:p.Val647Phe