Canonical Allele Identifier: CA2614916533

Gene: LRRC51 LRTOMT

Linked Data

• gnomAD v4: 11-72080709-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080712del , CM000673.2:g.72080712del	GRCh38
NC_000011.9:g.71791758del , CM000673.1:g.71791758del	GRCh37
NC_000011.8:g.71469406del	NCBI36
NG_021423.1:g.5377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-313del (LRRC51)	ENSP00000289488.2:n.-313del
ENST00000535883.6:c.-190del (LRRC51)	ENSP00000437561.1:n.-190del
ENST00000538413.6:c.-229del (LRRC51)	ENSP00000438762.2:n.-229del
ENST00000539271.6:c.-383del (LRRC51)	ENSP00000442267.2:n.-383del
ENST00000642510.1:c.-506del (LRRC51)	ENSP00000496544.1:n.-506del
ENST00000642648.1:c.-190del (LRRC51)	ENSP00000494362.1:n.-190del
ENST00000642813.1:n.147del (LRRC51)
ENST00000647530.1:c.-476del (LRRC51)	ENSP00000494072.1:n.-476del
ENST00000289488.6:c.-313del (LRRC51)	ENSP00000289488.2:n.-313del
ENST00000307198.11:c.-495del (LRRC51)	ENSP00000305742.7:n.-495del
ENST00000535883.5:c.-313del (LRRC51)	ENSP00000437561.1:n.-313del
ENST00000538413.5:c.-190del (LRRC51)	ENSP00000438762.1:n.-190del
NM_001145307.4:c.-313del (LRTOMT)	NP_001138779.1:n.-313del
NM_001145308.4:c.-495del (LRTOMT)	NP_001138780.1:n.-495del
NM_001145309.3:c.-716del (LRTOMT)	NP_001138781.1:n.-716del
NM_001145310.3:c.-716del (LRTOMT)	NP_001138782.1:n.-716del
NM_001205138.3:c.-230del (LRTOMT)	NP_001192067.1:n.-230del
NM_001271471.2:c.-313del (LRTOMT)	NP_001258400.1:n.-313del
NM_145309.5:c.-313del (LRTOMT)	NP_660352.1:n.-313del
NR_026886.3:n.382del (LRTOMT)
XM_006718473.2:c.-190del (LRTOMT)	XP_006718536.1:n.-190del
NM_001318803.1:c.-270del (LRTOMT)	NP_001305732.1:n.-270del
NR_134858.1:n.382del (LRTOMT)
XM_006718473.4:c.-190del (LRTOMT)	XP_006718536.1:n.-190del
XM_006718474.4:c.-229del (LRTOMT)	XP_006718537.1:n.-229del
XM_011544848.3:c.-476del (LRTOMT)	XP_011543150.1:n.-476del