Canonical Allele Identifier: CA475864912

Gene: TOMT LRTOMT LRRC51

Linked Data

• MyVariant Identifiers: chr11:g.71817201C>G (hg19)
• PubMed: PMID:28263302

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72106155C>G , CM000673.2:g.72106155C>G	GRCh38
NC_000011.9:g.71817201C>G , CM000673.1:g.71817201C>G	GRCh37
NC_000011.8:g.71494849C>G	NCBI36
NG_021423.1:g.30820C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.204C>G (TOMT) MANE Select	ENSP00000494667.1:p.Thr68=
ENST00000541899.2:c.204C>G (TOMT)	ENSP00000494667.1:p.Thr68=
ENST00000643715.1:c.438-2450C>G (LRTOMT)	ENSP00000496019.1:n.438-2450C>G
ENST00000646163.1:c.*22C>G (LRTOMT)	ENSP00000494749.1:n.*22C>G
ENST00000307198.11:c.303C>G (LRRC51)	ENSP00000305742.7:p.Thr101=
ENST00000419228.2:c.183C>G (LRRC51)	ENSP00000392233.2:p.Thr61=
ENST00000427369.6:c.*22C>G (LRRC51)	ENSP00000409403.2:n.*22C>G
ENST00000435085.5:c.303C>G (LRRC51)	ENSP00000409789.1:p.Thr101=
ENST00000439209.5:c.438-2450C>G (LRRC51)	ENSP00000395139.1:n.438-2450C>G
ENST00000541899.1:n.361C>G (LRRC51)
ENST00000544409.5:c.*22C>G (LRRC51)	ENSP00000440969.1:n.*22C>G
NM_001145308.4:c.303C>G (LRTOMT)	NP_001138780.1:p.Thr101=
NM_001145309.3:c.303C>G (LRTOMT)	NP_001138781.1:p.Thr101=
NM_001145310.3:c.183C>G (LRTOMT)	NP_001138782.1:p.Thr61=
XM_011544849.1:c.528C>G (LRTOMT)	XP_011543151.1:p.Thr176=
XM_024448401.1:c.528C>G (LRTOMT)	XP_024304169.1:p.Thr176=
NM_001145308.5:c.303C>G (LRTOMT)	NP_001138780.1:p.Thr101=
NM_001145309.4:c.303C>G (LRTOMT)	NP_001138781.1:p.Thr101=
NM_001145310.4:c.183C>G (LRTOMT)	NP_001138782.1:p.Thr61=
NM_001393500.1:c.204C>G (TOMT)	NP_001380429.1:p.Thr68=
NM_001393500.2:c.204C>G (TOMT) MANE Select	NP_001380429.1:p.Thr68=