Canonical Allele Identifier: CA1740329

Gene: ELMOD3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85371131C>T , CM000664.2:g.85371131C>T	GRCh38
NC_000002.11:g.85598254C>T , CM000664.1:g.85598254C>T	GRCh37
NC_000002.10:g.85451765C>T	NCBI36
NG_051291.1:g.21738C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001135022.2:c.406C>T MANE Select	NP_001128494.1:p.Arg136Ter
ENST00000409013.8:c.406C>T MANE Select	ENSP00000387139.3:p.Arg136Ter
NM_001135021.1:c.406C>T	NP_001128493.1:p.Arg136Ter
NM_001135021.2:c.406C>T	NP_001128493.1:p.Arg136Ter
NM_001135022.1:c.406C>T	NP_001128494.1:p.Arg136Ter
NM_001135023.1:c.406C>T	NP_001128495.1:p.Arg136Ter
NM_001135023.2:c.406C>T	NP_001128495.1:p.Arg136Ter
NM_001329791.1:c.406C>T	NP_001316720.1:p.Arg136Ter
NM_001329791.2:c.406C>T	NP_001316720.1:p.Arg136Ter
NM_001329792.1:c.406C>T	NP_001316721.1:p.Arg136Ter
NM_001329792.2:c.406C>T	NP_001316721.1:p.Arg136Ter
NM_001329793.1:c.406C>T	NP_001316722.1:p.Arg136Ter
NM_001329793.2:c.406C>T	NP_001316722.1:p.Arg136Ter
NM_032213.4:c.406C>T	NP_115589.2:p.Arg136Ter
NR_138131.1:n.843C>T
NR_138131.2:n.794C>T
NR_138132.1:n.1185C>T
NR_138132.2:n.1136C>T
NR_138133.1:n.748C>T
NR_138133.2:n.699C>T
ENST00000315658.11:c.406C>T	ENSP00000318264.7:p.Arg136Ter
ENST00000393852.8:c.406C>T	ENSP00000377434.4:p.Arg136Ter
ENST00000409013.7:c.406C>T	ENSP00000387139.3:p.Arg136Ter
ENST00000409331.6:c.406C>T	ENSP00000386257.2:p.Arg136Ter
ENST00000409344.7:c.406C>T	ENSP00000386248.3:p.Arg136Ter
ENST00000409890.6:c.406C>T	ENSP00000386304.2:p.Arg136Ter
ENST00000410106.5:c.406C>T	ENSP00000387134.1:p.Arg136Ter
ENST00000414593.5:c.406C>T	ENSP00000394774.1:p.Arg136Ter
ENST00000423095.7:c.406C>T	ENSP00000408745.3:p.Arg136Ter
ENST00000429764.5:c.175C>T	ENSP00000408329.1:p.Arg59Ter
ENST00000440462.5:c.*201C>T	ENSP00000398264.1:n.*201C>T
ENST00000444108.7:c.406C>T	ENSP00000401984.2:p.Arg136Ter
ENST00000446464.7:c.406C>T	ENSP00000407599.3:p.Arg136Ter
ENST00000488150.1:n.305C>T
ENST00000490508.5:n.618C>T
XM_005264596.2:c.406C>T	XP_005264653.1:p.Arg136Ter
XM_005264597.2:c.406C>T	XP_005264654.1:p.Arg136Ter
XM_005264598.2:c.406C>T	XP_005264655.1:p.Arg136Ter
XM_006712116.1:c.406C>T	XP_006712179.1:p.Arg136Ter
XM_024453169.1:c.406C>T	XP_024308937.1:p.Arg136Ter
XM_024453170.1:c.406C>T	XP_024308938.1:p.Arg136Ter
XM_024453171.1:c.406C>T	XP_024308939.1:p.Arg136Ter
XM_024453172.1:c.406C>T	XP_024308940.1:p.Arg136Ter
XR_001738978.1:n.887C>T
XR_001738979.1:n.792C>T
XR_426997.1:n.557C>T