Canonical Allele Identifier: CA600242553

Gene: LRTOMT LRRC51

Linked Data

• dbSNP Id: rs1301648701
• gnomAD v2: 11-71816780-T-G
• gnomAD v3: 11-72105734-T-G
• gnomAD v4: 11-72105734-T-G
• MyVariant Identifiers: chr11:g.71816780T>G (hg19) ; chr11:g.72105734T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72105734T>G , CM000673.2:g.72105734T>G	GRCh38
NC_000011.9:g.71816780T>G , CM000673.1:g.71816780T>G	GRCh37
NC_000011.8:g.71494428T>G	NCBI36
NG_021423.1:g.30399T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643715.1:c.438-2871T>G (LRTOMT)	ENSP00000496019.1:n.438-2871T>G
ENST00000646163.1:c.73-322T>G (LRTOMT)	ENSP00000494749.1:n.73-322T>G
ENST00000307198.11:c.84-202T>G (LRRC51)	ENSP00000305742.7:n.84-202T>G
ENST00000419228.2:c.84-322T>G (LRRC51)	ENSP00000392233.2:n.84-322T>G
ENST00000427369.6:c.487-202T>G (LRRC51)	ENSP00000409403.2:n.487-202T>G
ENST00000435085.5:c.84-202T>G (LRRC51)	ENSP00000409789.1:n.84-202T>G
ENST00000439209.5:c.438-2871T>G (LRRC51)	ENSP00000395139.1:n.438-2871T>G
ENST00000544409.5:c.487-322T>G (LRRC51)	ENSP00000440969.1:n.487-322T>G
NM_001145308.4:c.84-202T>G (LRTOMT)	NP_001138780.1:n.84-202T>G
NM_001145309.3:c.84-202T>G (LRTOMT)	NP_001138781.1:n.84-202T>G
NM_001145310.3:c.84-322T>G (LRTOMT)	NP_001138782.1:n.84-322T>G
XM_011544849.1:c.309-202T>G (LRTOMT)	XP_011543151.1:n.309-202T>G
XM_024448401.1:c.309-202T>G (LRTOMT)	XP_024304169.1:n.309-202T>G
NM_001145308.5:c.84-202T>G (LRTOMT)	NP_001138780.1:n.84-202T>G
NM_001145309.4:c.84-202T>G (LRTOMT)	NP_001138781.1:n.84-202T>G
NM_001145310.4:c.84-322T>G (LRTOMT)	NP_001138782.1:n.84-322T>G