Canonical Allele Identifier: CA939427222

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1944114998
• gnomAD v3: 11-72080835-G-C
• gnomAD v4: 11-72080835-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080835G>C , CM000673.2:g.72080835G>C	GRCh38
NC_000011.9:g.71791881G>C , CM000673.1:g.71791881G>C	GRCh37
NC_000011.8:g.71469529G>C	NCBI36
NG_021423.1:g.5500G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-190G>C (LRRC51)	ENSP00000289488.2:n.-190G>C
ENST00000535883.6:c.-140+73G>C (LRRC51)	ENSP00000437561.1:n.-140+73G>C
ENST00000538413.6:c.-106G>C (LRRC51)	ENSP00000438762.2:n.-106G>C
ENST00000539271.6:c.-333+73G>C (LRRC51)	ENSP00000442267.2:n.-333+73G>C
ENST00000539587.6:c.-177G>C (LRRC51)	ENSP00000437649.2:n.-177G>C
ENST00000642510.1:c.-383G>C (LRRC51)	ENSP00000496544.1:n.-383G>C
ENST00000642648.1:c.-140+73G>C (LRRC51)	ENSP00000494362.1:n.-140+73G>C
ENST00000642813.1:n.270G>C (LRRC51)
ENST00000646163.1:c.-383G>C (LRTOMT)	ENSP00000494749.1:n.-383G>C
ENST00000647530.1:c.-353G>C (LRRC51)	ENSP00000494072.1:n.-353G>C
ENST00000289488.6:c.-190G>C (LRRC51)	ENSP00000289488.2:n.-190G>C
ENST00000307198.11:c.-372G>C (LRRC51)	ENSP00000305742.7:n.-372G>C
ENST00000412777.6:n.59G>C (LRRC51)
ENST00000423494.6:c.-107G>C (LRRC51)	ENSP00000441249.1:n.-107G>C
ENST00000535883.5:c.-190G>C (LRRC51)	ENSP00000437561.1:n.-190G>C
ENST00000538413.5:c.-140+73G>C (LRRC51)	ENSP00000438762.1:n.-140+73G>C
ENST00000539271.5:c.-372G>C (LRRC51)	ENSP00000442267.1:n.-372G>C
ENST00000539587.5:c.-166G>C (LRRC51)	ENSP00000437649.1:n.-166G>C
NM_001145307.4:c.-190G>C (LRTOMT)	NP_001138779.1:n.-190G>C
NM_001145308.4:c.-372G>C (LRTOMT)	NP_001138780.1:n.-372G>C
NM_001145309.3:c.-593G>C (LRTOMT)	NP_001138781.1:n.-593G>C
NM_001145310.3:c.-593G>C (LRTOMT)	NP_001138782.1:n.-593G>C
NM_001205138.3:c.-107G>C (LRTOMT)	NP_001192067.1:n.-107G>C
NM_001271471.2:c.-190G>C (LRTOMT)	NP_001258400.1:n.-190G>C
NM_145309.5:c.-190G>C (LRTOMT)	NP_660352.1:n.-190G>C
NR_026886.3:n.505G>C (LRTOMT)
XM_006718472.2:c.-147G>C (LRTOMT)	XP_006718535.1:n.-147G>C
XM_006718473.2:c.-140+73G>C (LRTOMT)	XP_006718536.1:n.-140+73G>C
XM_006718474.2:c.-106G>C (LRTOMT)	XP_006718537.1:n.-106G>C
XM_011544847.1:c.-295G>C (LRTOMT)	XP_011543149.1:n.-295G>C
XM_011544848.1:c.-353G>C (LRTOMT)	XP_011543150.1:n.-353G>C
NM_001318803.1:c.-147G>C (LRTOMT)	NP_001305732.1:n.-147G>C
NR_134858.1:n.505G>C (LRTOMT)
XM_006718473.4:c.-140+73G>C (LRTOMT)	XP_006718536.1:n.-140+73G>C
XM_006718474.4:c.-106G>C (LRTOMT)	XP_006718537.1:n.-106G>C
XM_011544847.3:c.-295G>C (LRTOMT)	XP_011543149.1:n.-295G>C
XM_011544848.3:c.-353G>C (LRTOMT)	XP_011543150.1:n.-353G>C