Canonical Allele Identifier: CA2614916592

Gene: LRRC51 LRTOMT

Linked Data

• gnomAD v4: 11-72080733-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080733A>G , CM000673.2:g.72080733A>G	GRCh38
NC_000011.9:g.71791779A>G , CM000673.1:g.71791779A>G	GRCh37
NC_000011.8:g.71469427A>G	NCBI36
NG_021423.1:g.5398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-292A>G (LRRC51)	ENSP00000289488.2:n.-292A>G
ENST00000535883.6:c.-169A>G (LRRC51)	ENSP00000437561.1:n.-169A>G
ENST00000538413.6:c.-208A>G (LRRC51)	ENSP00000438762.2:n.-208A>G
ENST00000539271.6:c.-362A>G (LRRC51)	ENSP00000442267.2:n.-362A>G
ENST00000642510.1:c.-485A>G (LRRC51)	ENSP00000496544.1:n.-485A>G
ENST00000642648.1:c.-169A>G (LRRC51)	ENSP00000494362.1:n.-169A>G
ENST00000642813.1:n.168A>G (LRRC51)
ENST00000647530.1:c.-455A>G (LRRC51)	ENSP00000494072.1:n.-455A>G
ENST00000289488.6:c.-292A>G (LRRC51)	ENSP00000289488.2:n.-292A>G
ENST00000307198.11:c.-474A>G (LRRC51)	ENSP00000305742.7:n.-474A>G
ENST00000535883.5:c.-292A>G (LRRC51)	ENSP00000437561.1:n.-292A>G
ENST00000538413.5:c.-169A>G (LRRC51)	ENSP00000438762.1:n.-169A>G
NM_001145307.4:c.-292A>G (LRTOMT)	NP_001138779.1:n.-292A>G
NM_001145308.4:c.-474A>G (LRTOMT)	NP_001138780.1:n.-474A>G
NM_001145309.3:c.-695A>G (LRTOMT)	NP_001138781.1:n.-695A>G
NM_001145310.3:c.-695A>G (LRTOMT)	NP_001138782.1:n.-695A>G
NM_001205138.3:c.-209A>G (LRTOMT)	NP_001192067.1:n.-209A>G
NM_001271471.2:c.-292A>G (LRTOMT)	NP_001258400.1:n.-292A>G
NM_145309.5:c.-292A>G (LRTOMT)	NP_660352.1:n.-292A>G
NR_026886.3:n.403A>G (LRTOMT)
XM_006718473.2:c.-169A>G (LRTOMT)	XP_006718536.1:n.-169A>G
NM_001318803.1:c.-249A>G (LRTOMT)	NP_001305732.1:n.-249A>G
NR_134858.1:n.403A>G (LRTOMT)
XM_006718473.4:c.-169A>G (LRTOMT)	XP_006718536.1:n.-169A>G
XM_006718474.4:c.-208A>G (LRTOMT)	XP_006718537.1:n.-208A>G
XM_011544848.3:c.-455A>G (LRTOMT)	XP_011543150.1:n.-455A>G