Canonical Allele Identifier: CA1981828485

Gene: LRRC51 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080731G= , CM000673.2:g.72080731G=	GRCh38
NC_000011.9:g.71791777G= , CM000673.1:g.71791777G=	GRCh37
NC_000011.8:g.71469425G=	NCBI36
NG_021423.1:g.5396G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-294G= (LRRC51)	ENSP00000289488.2:n.-294G=
ENST00000535883.6:c.-171G= (LRRC51)	ENSP00000437561.1:n.-171G=
ENST00000538413.6:c.-210G= (LRRC51)	ENSP00000438762.2:n.-210G=
ENST00000539271.6:c.-364G= (LRRC51)	ENSP00000442267.2:n.-364G=
ENST00000642510.1:c.-487G= (LRRC51)	ENSP00000496544.1:n.-487G=
ENST00000642648.1:c.-171G= (LRRC51)	ENSP00000494362.1:n.-171G=
ENST00000642813.1:n.166G= (LRRC51)
ENST00000647530.1:c.-457G= (LRRC51)	ENSP00000494072.1:n.-457G=
ENST00000289488.6:c.-294G= (LRRC51)	ENSP00000289488.2:n.-294G=
ENST00000307198.11:c.-476G= (LRRC51)	ENSP00000305742.7:n.-476G=
ENST00000535883.5:c.-294G= (LRRC51)	ENSP00000437561.1:n.-294G=
ENST00000538413.5:c.-171G= (LRRC51)	ENSP00000438762.1:n.-171G=
NM_001145307.4:c.-294G= (LRTOMT)	NP_001138779.1:n.-294G=
NM_001145308.4:c.-476G= (LRTOMT)	NP_001138780.1:n.-476G=
NM_001145309.3:c.-697G= (LRTOMT)	NP_001138781.1:n.-697G=
NM_001145310.3:c.-697G= (LRTOMT)	NP_001138782.1:n.-697G=
NM_001205138.3:c.-211G= (LRTOMT)	NP_001192067.1:n.-211G=
NM_001271471.2:c.-294G= (LRTOMT)	NP_001258400.1:n.-294G=
NM_145309.5:c.-294G= (LRTOMT)	NP_660352.1:n.-294G=
NR_026886.3:n.401G= (LRTOMT)
XM_006718473.2:c.-171G= (LRTOMT)	XP_006718536.1:n.-171G=
NM_001318803.1:c.-251G= (LRTOMT)	NP_001305732.1:n.-251G=
NR_134858.1:n.401G= (LRTOMT)
XM_006718473.4:c.-171G= (LRTOMT)	XP_006718536.1:n.-171G=
XM_006718474.4:c.-210G= (LRTOMT)	XP_006718537.1:n.-210G=
XM_011544848.3:c.-457G= (LRTOMT)	XP_011543150.1:n.-457G=