Canonical Allele Identifier: CA381717535

Gene: TOMT LRTOMT LRRC51

Linked Data

• ClinVar Variation Id: 2241403
• ClinVar RCV Id: RCV002719468
• dbSNP Id: rs1212150176
• gnomAD v3: 11-72106052-G-A
• gnomAD v4: 11-72106052-G-A
• COSMIC: COSM1585999
• MyVariant Identifiers: chr11:g.71817098G>A (hg19) ; chr11:g.72106052G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72106052G>A , CM000673.2:g.72106052G>A	GRCh38
NC_000011.9:g.71817098G>A , CM000673.1:g.71817098G>A	GRCh37
NC_000011.8:g.71494746G>A	NCBI36
NG_021423.1:g.30717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.101G>A (TOMT) MANE Select	ENSP00000494667.1:p.Arg34Gln
ENST00000541899.2:c.101G>A (TOMT)	ENSP00000494667.1:p.Arg34Gln
ENST00000643715.1:c.438-2553G>A (LRTOMT)	ENSP00000496019.1:n.438-2553G>A
ENST00000646163.1:c.73-4G>A (LRTOMT)	ENSP00000494749.1:n.73-4G>A
ENST00000307198.11:c.200G>A (LRRC51)	ENSP00000305742.7:p.Arg67Gln
ENST00000419228.2:c.84-4G>A (LRRC51)	ENSP00000392233.2:n.84-4G>A
ENST00000427369.6:c.603G>A (LRRC51)	ENSP00000409403.2:p.Ala201=
ENST00000435085.5:c.200G>A (LRRC51)	ENSP00000409789.1:p.Arg67Gln
ENST00000439209.5:c.438-2553G>A (LRRC51)	ENSP00000395139.1:n.438-2553G>A
ENST00000541899.1:n.258G>A (LRRC51)
ENST00000544409.5:c.487-4G>A (LRRC51)	ENSP00000440969.1:n.487-4G>A
NM_001145308.4:c.200G>A (LRTOMT)	NP_001138780.1:p.Arg67Gln
NM_001145309.3:c.200G>A (LRTOMT)	NP_001138781.1:p.Arg67Gln
NM_001145310.3:c.84-4G>A (LRTOMT)	NP_001138782.1:n.84-4G>A
XM_011544849.1:c.425G>A (LRTOMT)	XP_011543151.1:p.Arg142Gln
XM_024448401.1:c.425G>A (LRTOMT)	XP_024304169.1:p.Arg142Gln
NM_001145308.5:c.200G>A (LRTOMT)	NP_001138780.1:p.Arg67Gln
NM_001145309.4:c.200G>A (LRTOMT)	NP_001138781.1:p.Arg67Gln
NM_001145310.4:c.84-4G>A (LRTOMT)	NP_001138782.1:n.84-4G>A
NM_001393500.1:c.101G>A (TOMT)	NP_001380429.1:p.Arg34Gln
NM_001393500.2:c.101G>A (TOMT) MANE Select	NP_001380429.1:p.Arg34Gln