Canonical Allele Identifier: CA375765890

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140652374C>A (hg19) ; chr9:g.137757922C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137757922C>A , CM000671.2:g.137757922C>A	GRCh38
NC_000009.11:g.140652374C>A , CM000671.1:g.140652374C>A	GRCh37
NC_000009.10:g.139772195C>A	NCBI36
NG_011776.1:g.143931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1412C>A MANE Select	ENSP00000417980.1:p.Thr471Lys
ENST00000629335.2:c.1412C>A	ENSP00000490056.1:p.Thr471Lys
ENST00000636027.1:c.1298C>A	ENSP00000489961.1:p.Thr433Lys
ENST00000637161.1:c.1319C>A	ENSP00000490328.1:p.Thr440Lys
ENST00000637261.1:c.1452C>A	ENSP00000490815.1:n.1452C>A
ENST00000637977.1:c.1357C>A
ENST00000638071.1:c.1039C>A
ENST00000640639.1:c.581C>A	ENSP00000491823.1:p.Thr194Lys
ENST00000371394.6:c.*1147C>A	ENSP00000485945.1:n.*1147C>A
ENST00000460843.5:c.1412C>A	ENSP00000417980.1:p.Thr471Lys
ENST00000462484.5:c.1412C>A	ENSP00000417328.1:p.Thr471Lys
ENST00000462942.3:c.269C>A	ENSP00000436107.1:p.Thr90Lys
ENST00000465566.2:c.104C>A	ENSP00000486261.1:p.Thr35Lys
ENST00000629808.2:c.505C>A
NM_001145527.1:c.1412C>A	NP_001138999.1:p.Thr471Lys
NM_024757.4:c.1412C>A	NP_079033.4:p.Thr471Lys
XM_005266105.3:c.1403C>A	XP_005266162.1:p.Thr468Lys
XM_005266110.1:c.1319C>A	XP_005266167.1:p.Thr440Lys
XM_006717288.2:c.1394C>A	XP_006717351.1:p.Thr465Lys
XM_011519021.1:c.1421C>A	XP_011517323.1:p.Thr474Lys
XM_011519022.1:c.1418C>A	XP_011517324.1:p.Thr473Lys
XM_011519023.1:c.1400C>A	XP_011517325.1:p.Thr467Lys
XM_011519024.1:c.1343C>A	XP_011517326.1:p.Thr448Lys
XM_011519025.1:c.1319C>A	XP_011517327.1:p.Thr440Lys
XM_011519026.1:c.1421C>A	XP_011517328.1:p.Thr474Lys
XM_011519027.1:c.1421C>A	XP_011517329.1:p.Thr474Lys
XM_011519028.1:c.1421C>A	XP_011517330.1:p.Thr474Lys
XM_011519033.1:c.1400C>A	XP_011517335.1:p.Thr467Lys
NM_001354259.1:c.1319C>A	NP_001341188.1:p.Thr440Lys
NM_001354263.1:c.1391C>A	NP_001341192.1:p.Thr464Lys
NM_001354611.1:c.1412C>A	NP_001341540.1:p.Thr471Lys
NM_001354612.1:c.1319C>A	NP_001341541.1:p.Thr440Lys
XM_005266105.5:c.1403C>A	XP_005266162.1:p.Thr468Lys
XM_011519021.3:c.1421C>A	XP_011517323.1:p.Thr474Lys
XM_011519022.3:c.1418C>A	XP_011517324.1:p.Thr473Lys
XM_011519023.3:c.1400C>A	XP_011517325.1:p.Thr467Lys
XM_017015134.1:c.1397C>A	XP_016870623.1:p.Thr466Lys
XM_017015136.2:c.1313C>A	XP_016870625.1:p.Thr438Lys
XM_017015137.1:c.1298C>A	XP_016870626.1:p.Thr433Lys
XM_017015138.1:c.1298C>A	XP_016870627.1:p.Thr433Lys
XM_024447674.1:c.1241C>A	XP_024303442.1:p.Thr414Lys
XM_024447675.1:c.1319C>A	XP_024303443.1:p.Thr440Lys
XM_024447676.1:c.536C>A	XP_024303444.1:p.Thr179Lys
XM_024447677.1:c.536C>A	XP_024303445.1:p.Thr179Lys
XM_024447678.1:c.1319C>A	XP_024303446.1:p.Thr440Lys
XM_024447679.1:c.1319C>A	XP_024303447.1:p.Thr440Lys
XM_024447680.1:c.1298C>A	XP_024303448.1:p.Thr433Lys
NM_024757.5:c.1412C>A MANE Select	NP_079033.4:p.Thr471Lys
NM_001145527.2:c.1412C>A	NP_001138999.1:p.Thr471Lys
NM_001354259.2:c.1319C>A	NP_001341188.1:p.Thr440Lys
NM_001354263.2:c.1391C>A	NP_001341192.1:p.Thr464Lys
NM_001354611.2:c.1412C>A	NP_001341540.1:p.Thr471Lys
NM_001354612.2:c.1319C>A	NP_001341541.1:p.Thr440Lys