Canonical Allele Identifier: CA475864763

Gene: TOMT LRTOMT LRRC51

Linked Data

• MyVariant Identifiers: chr11:g.71817021C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72105975C>A , CM000673.2:g.72105975C>A	GRCh38
NC_000011.9:g.71817021C>A , CM000673.1:g.71817021C>A	GRCh37
NC_000011.8:g.71494669C>A	NCBI36
NG_021423.1:g.30640C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.24C>A (TOMT) MANE Select	ENSP00000494667.1:p.Ala8=
ENST00000541899.2:c.24C>A (TOMT)	ENSP00000494667.1:p.Ala8=
ENST00000643715.1:c.438-2630C>A (LRTOMT)	ENSP00000496019.1:n.438-2630C>A
ENST00000646163.1:c.73-81C>A (LRTOMT)	ENSP00000494749.1:n.73-81C>A
ENST00000307198.11:c.123C>A (LRRC51)	ENSP00000305742.7:p.Ala41=
ENST00000419228.2:c.84-81C>A (LRRC51)	ENSP00000392233.2:n.84-81C>A
ENST00000427369.6:c.526C>A (LRRC51)	ENSP00000409403.2:p.Leu176Ile
ENST00000435085.5:c.123C>A (LRRC51)	ENSP00000409789.1:p.Ala41=
ENST00000439209.5:c.438-2630C>A (LRRC51)	ENSP00000395139.1:n.438-2630C>A
ENST00000541899.1:n.181C>A (LRRC51)
ENST00000544409.5:c.487-81C>A (LRRC51)	ENSP00000440969.1:n.487-81C>A
NM_001145308.4:c.123C>A (LRTOMT)	NP_001138780.1:p.Ala41=
NM_001145309.3:c.123C>A (LRTOMT)	NP_001138781.1:p.Ala41=
NM_001145310.3:c.84-81C>A (LRTOMT)	NP_001138782.1:n.84-81C>A
XM_011544849.1:c.348C>A (LRTOMT)	XP_011543151.1:p.Ala116=
XM_024448401.1:c.348C>A (LRTOMT)	XP_024304169.1:p.Ala116=
NM_001145308.5:c.123C>A (LRTOMT)	NP_001138780.1:p.Ala41=
NM_001145309.4:c.123C>A (LRTOMT)	NP_001138781.1:p.Ala41=
NM_001145310.4:c.84-81C>A (LRTOMT)	NP_001138782.1:n.84-81C>A
NM_001393500.1:c.24C>A (TOMT)	NP_001380429.1:p.Ala8=
NM_001393500.2:c.24C>A (TOMT) MANE Select	NP_001380429.1:p.Ala8=