Canonical Allele Identifier: CA679952974

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1396721124
• gnomAD v3: 11-72080853-G-A
• gnomAD v4: 11-72080853-G-A
• MyVariant Identifiers: chr11:g.71791899G>A (hg19) ; chr11:g.72080853G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080853G>A , CM000673.2:g.72080853G>A	GRCh38
NC_000011.9:g.71791899G>A , CM000673.1:g.71791899G>A	GRCh37
NC_000011.8:g.71469547G>A	NCBI36
NG_021423.1:g.5518G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.8:c.-172G>A (LRRC51) MANE Select	ENSP00000289488.2:n.-172G>A
ENST00000289488.7:c.-172G>A (LRRC51)	ENSP00000289488.2:n.-172G>A
ENST00000535883.6:c.-140+91G>A (LRRC51)	ENSP00000437561.1:n.-140+91G>A
ENST00000536917.2:c.-129G>A (LRRC51)	ENSP00000443421.1:n.-129G>A
ENST00000538413.6:c.-88G>A (LRRC51)	ENSP00000438762.2:n.-88G>A
ENST00000539271.6:c.-333+91G>A (LRRC51)	ENSP00000442267.2:n.-333+91G>A
ENST00000539587.6:c.-159G>A (LRRC51)	ENSP00000437649.2:n.-159G>A
ENST00000642510.1:c.-365G>A (LRRC51)	ENSP00000496544.1:n.-365G>A
ENST00000642648.1:c.-140+91G>A (LRRC51)	ENSP00000494362.1:n.-140+91G>A
ENST00000642813.1:n.288G>A (LRRC51)
ENST00000643715.1:c.-129G>A (LRTOMT)	ENSP00000496019.1:n.-129G>A
ENST00000645358.1:c.-129G>A (LRRC51)	ENSP00000495121.1:n.-129G>A
ENST00000646163.1:c.-365G>A (LRTOMT)	ENSP00000494749.1:n.-365G>A
ENST00000647530.1:c.-335G>A (LRRC51)	ENSP00000494072.1:n.-335G>A
ENST00000289488.6:c.-172G>A (LRRC51)	ENSP00000289488.2:n.-172G>A
ENST00000307198.11:c.-354G>A (LRRC51)	ENSP00000305742.7:n.-354G>A
ENST00000412777.6:n.77G>A (LRRC51)
ENST00000423494.6:c.-89G>A (LRRC51)	ENSP00000441249.1:n.-89G>A
ENST00000535883.5:c.-172G>A (LRRC51)	ENSP00000437561.1:n.-172G>A
ENST00000538413.5:c.-140+91G>A (LRRC51)	ENSP00000438762.1:n.-140+91G>A
ENST00000538478.5:c.-129G>A (LRRC51)	ENSP00000444583.1:n.-129G>A
ENST00000539271.5:c.-354G>A (LRRC51)	ENSP00000442267.1:n.-354G>A
ENST00000539587.5:c.-148G>A (LRRC51)	ENSP00000437649.1:n.-148G>A
NM_001145307.4:c.-172G>A (LRTOMT)	NP_001138779.1:n.-172G>A
NM_001145308.4:c.-354G>A (LRTOMT)	NP_001138780.1:n.-354G>A
NM_001145309.3:c.-575G>A (LRTOMT)	NP_001138781.1:n.-575G>A
NM_001145310.3:c.-575G>A (LRTOMT)	NP_001138782.1:n.-575G>A
NM_001205138.3:c.-89G>A (LRTOMT)	NP_001192067.1:n.-89G>A
NM_001271471.2:c.-172G>A (LRTOMT)	NP_001258400.1:n.-172G>A
NM_145309.5:c.-172G>A (LRTOMT)	NP_660352.1:n.-172G>A
NR_026886.3:n.523G>A (LRTOMT)
XM_006718472.2:c.-129G>A (LRTOMT)	XP_006718535.1:n.-129G>A
XM_006718473.2:c.-140+91G>A (LRTOMT)	XP_006718536.1:n.-140+91G>A
XM_006718474.2:c.-88G>A (LRTOMT)	XP_006718537.1:n.-88G>A
XM_011544847.1:c.-277G>A (LRTOMT)	XP_011543149.1:n.-277G>A
XM_011544848.1:c.-335G>A (LRTOMT)	XP_011543150.1:n.-335G>A
NM_001318803.1:c.-129G>A (LRTOMT)	NP_001305732.1:n.-129G>A
NR_134858.1:n.523G>A (LRTOMT)
XM_006718473.4:c.-140+91G>A (LRTOMT)	XP_006718536.1:n.-140+91G>A
XM_006718474.4:c.-88G>A (LRTOMT)	XP_006718537.1:n.-88G>A
XM_011544847.3:c.-277G>A (LRTOMT)	XP_011543149.1:n.-277G>A
XM_011544848.3:c.-335G>A (LRTOMT)	XP_011543150.1:n.-335G>A
NM_001145307.5:c.-172G>A (LRTOMT)	NP_001138779.1:n.-172G>A
NM_001145308.5:c.-354G>A (LRTOMT)	NP_001138780.1:n.-354G>A
NM_001145309.4:c.-575G>A (LRTOMT)	NP_001138781.1:n.-575G>A
NM_001145310.4:c.-575G>A (LRTOMT)	NP_001138782.1:n.-575G>A
NM_001205138.4:c.-89G>A (LRTOMT)	NP_001192067.1:n.-89G>A
NM_001271471.3:c.-172G>A (LRTOMT)	NP_001258400.1:n.-172G>A
NM_001318803.2:c.-129G>A (LRTOMT)	NP_001305732.1:n.-129G>A
NM_145309.6:c.-172G>A (LRTOMT) MANE Select	NP_660352.1:n.-172G>A
NR_026886.4:n.4G>A (LRTOMT)