Canonical Allele Identifier: CA600242561

Gene: LRTOMT LRRC51

Linked Data

• dbSNP Id: rs1388269705
• gnomAD v2: 11-71816933-T-C
• gnomAD v4: 11-72105887-T-C
• MyVariant Identifiers: chr11:g.71816933T>C (hg19) ; chr11:g.72105887T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72105887T>C , CM000673.2:g.72105887T>C	GRCh38
NC_000011.9:g.71816933T>C , CM000673.1:g.71816933T>C	GRCh37
NC_000011.8:g.71494581T>C	NCBI36
NG_021423.1:g.30552T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643715.1:c.438-2718T>C (LRTOMT)	ENSP00000496019.1:n.438-2718T>C
ENST00000646163.1:c.73-169T>C (LRTOMT)	ENSP00000494749.1:n.73-169T>C
ENST00000307198.11:c.84-49T>C (LRRC51)	ENSP00000305742.7:n.84-49T>C
ENST00000419228.2:c.84-169T>C (LRRC51)	ENSP00000392233.2:n.84-169T>C
ENST00000427369.6:c.487-49T>C (LRRC51)	ENSP00000409403.2:n.487-49T>C
ENST00000435085.5:c.84-49T>C (LRRC51)	ENSP00000409789.1:n.84-49T>C
ENST00000439209.5:c.438-2718T>C (LRRC51)	ENSP00000395139.1:n.438-2718T>C
ENST00000541899.1:n.93T>C (LRRC51)
ENST00000544409.5:c.487-169T>C (LRRC51)	ENSP00000440969.1:n.487-169T>C
NM_001145308.4:c.84-49T>C (LRTOMT)	NP_001138780.1:n.84-49T>C
NM_001145309.3:c.84-49T>C (LRTOMT)	NP_001138781.1:n.84-49T>C
NM_001145310.3:c.84-169T>C (LRTOMT)	NP_001138782.1:n.84-169T>C
XM_011544849.1:c.309-49T>C (LRTOMT)	XP_011543151.1:n.309-49T>C
XM_024448401.1:c.309-49T>C (LRTOMT)	XP_024304169.1:n.309-49T>C
NM_001145308.5:c.84-49T>C (LRTOMT)	NP_001138780.1:n.84-49T>C
NM_001145309.4:c.84-49T>C (LRTOMT)	NP_001138781.1:n.84-49T>C
NM_001145310.4:c.84-169T>C (LRTOMT)	NP_001138782.1:n.84-169T>C