Canonical Allele Identifier: CA6168569

Gene: TOMT LRTOMT LRRC51

Linked Data

• dbSNP Id: rs766221873
• ExAC: 11:71817046 C / A
• gnomAD v2: 11-71817046-C-A
• gnomAD v4: 11-72106000-C-A
• MyVariant Identifiers: chr11:g.71817046C>A (hg19) ; chr11:g.72106000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72106000C>A , CM000673.2:g.72106000C>A	GRCh38
NC_000011.9:g.71817046C>A , CM000673.1:g.71817046C>A	GRCh37
NC_000011.8:g.71494694C>A	NCBI36
NG_021423.1:g.30665C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.49C>A (TOMT) MANE Select	ENSP00000494667.1:p.Leu17Met
ENST00000541899.2:c.49C>A (TOMT)	ENSP00000494667.1:p.Leu17Met
ENST00000643715.1:c.438-2605C>A (LRTOMT)	ENSP00000496019.1:n.438-2605C>A
ENST00000646163.1:c.73-56C>A (LRTOMT)	ENSP00000494749.1:n.73-56C>A
ENST00000307198.11:c.148C>A (LRRC51)	ENSP00000305742.7:p.Leu50Met
ENST00000419228.2:c.84-56C>A (LRRC51)	ENSP00000392233.2:n.84-56C>A
ENST00000427369.6:c.551C>A (LRRC51)	ENSP00000409403.2:p.Ala184Asp
ENST00000435085.5:c.148C>A (LRRC51)	ENSP00000409789.1:p.Leu50Met
ENST00000439209.5:c.438-2605C>A (LRRC51)	ENSP00000395139.1:n.438-2605C>A
ENST00000541899.1:n.206C>A (LRRC51)
ENST00000544409.5:c.487-56C>A (LRRC51)	ENSP00000440969.1:n.487-56C>A
NM_001145308.4:c.148C>A (LRTOMT)	NP_001138780.1:p.Leu50Met
NM_001145309.3:c.148C>A (LRTOMT)	NP_001138781.1:p.Leu50Met
NM_001145310.3:c.84-56C>A (LRTOMT)	NP_001138782.1:n.84-56C>A
XM_011544849.1:c.373C>A (LRTOMT)	XP_011543151.1:p.Leu125Met
XM_024448401.1:c.373C>A (LRTOMT)	XP_024304169.1:p.Leu125Met
NM_001145308.5:c.148C>A (LRTOMT)	NP_001138780.1:p.Leu50Met
NM_001145309.4:c.148C>A (LRTOMT)	NP_001138781.1:p.Leu50Met
NM_001145310.4:c.84-56C>A (LRTOMT)	NP_001138782.1:n.84-56C>A
NM_001393500.1:c.49C>A (TOMT)	NP_001380429.1:p.Leu17Met
NM_001393500.2:c.49C>A (TOMT) MANE Select	NP_001380429.1:p.Leu17Met