Canonical Allele Identifier: CA2614916585

Gene: LRRC51 LRTOMT

Linked Data

• gnomAD v4: 11-72080730-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080730T>C , CM000673.2:g.72080730T>C	GRCh38
NC_000011.9:g.71791776T>C , CM000673.1:g.71791776T>C	GRCh37
NC_000011.8:g.71469424T>C	NCBI36
NG_021423.1:g.5395T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-295T>C (LRRC51)	ENSP00000289488.2:n.-295T>C
ENST00000535883.6:c.-172T>C (LRRC51)	ENSP00000437561.1:n.-172T>C
ENST00000538413.6:c.-211T>C (LRRC51)	ENSP00000438762.2:n.-211T>C
ENST00000539271.6:c.-365T>C (LRRC51)	ENSP00000442267.2:n.-365T>C
ENST00000642510.1:c.-488T>C (LRRC51)	ENSP00000496544.1:n.-488T>C
ENST00000642648.1:c.-172T>C (LRRC51)	ENSP00000494362.1:n.-172T>C
ENST00000642813.1:n.165T>C (LRRC51)
ENST00000647530.1:c.-458T>C (LRRC51)	ENSP00000494072.1:n.-458T>C
ENST00000289488.6:c.-295T>C (LRRC51)	ENSP00000289488.2:n.-295T>C
ENST00000307198.11:c.-477T>C (LRRC51)	ENSP00000305742.7:n.-477T>C
ENST00000535883.5:c.-295T>C (LRRC51)	ENSP00000437561.1:n.-295T>C
ENST00000538413.5:c.-172T>C (LRRC51)	ENSP00000438762.1:n.-172T>C
NM_001145307.4:c.-295T>C (LRTOMT)	NP_001138779.1:n.-295T>C
NM_001145308.4:c.-477T>C (LRTOMT)	NP_001138780.1:n.-477T>C
NM_001145309.3:c.-698T>C (LRTOMT)	NP_001138781.1:n.-698T>C
NM_001145310.3:c.-698T>C (LRTOMT)	NP_001138782.1:n.-698T>C
NM_001205138.3:c.-212T>C (LRTOMT)	NP_001192067.1:n.-212T>C
NM_001271471.2:c.-295T>C (LRTOMT)	NP_001258400.1:n.-295T>C
NM_145309.5:c.-295T>C (LRTOMT)	NP_660352.1:n.-295T>C
NR_026886.3:n.400T>C (LRTOMT)
XM_006718473.2:c.-172T>C (LRTOMT)	XP_006718536.1:n.-172T>C
NM_001318803.1:c.-252T>C (LRTOMT)	NP_001305732.1:n.-252T>C
NR_134858.1:n.400T>C (LRTOMT)
XM_006718473.4:c.-172T>C (LRTOMT)	XP_006718536.1:n.-172T>C
XM_006718474.4:c.-211T>C (LRTOMT)	XP_006718537.1:n.-211T>C
XM_011544848.3:c.-458T>C (LRTOMT)	XP_011543150.1:n.-458T>C