Canonical Allele Identifier: CA1981828475

Gene: LRRC51 LRTOMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080716G= , CM000673.2:g.72080716G=	GRCh38
NC_000011.9:g.71791762G= , CM000673.1:g.71791762G=	GRCh37
NC_000011.8:g.71469410G=	NCBI36
NG_021423.1:g.5381G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-309G= (LRRC51)	ENSP00000289488.2:n.-309G=
ENST00000535883.6:c.-186G= (LRRC51)	ENSP00000437561.1:n.-186G=
ENST00000538413.6:c.-225G= (LRRC51)	ENSP00000438762.2:n.-225G=
ENST00000539271.6:c.-379G= (LRRC51)	ENSP00000442267.2:n.-379G=
ENST00000642510.1:c.-502G= (LRRC51)	ENSP00000496544.1:n.-502G=
ENST00000642648.1:c.-186G= (LRRC51)	ENSP00000494362.1:n.-186G=
ENST00000642813.1:n.151G= (LRRC51)
ENST00000647530.1:c.-472G= (LRRC51)	ENSP00000494072.1:n.-472G=
ENST00000289488.6:c.-309G= (LRRC51)	ENSP00000289488.2:n.-309G=
ENST00000307198.11:c.-491G= (LRRC51)	ENSP00000305742.7:n.-491G=
ENST00000535883.5:c.-309G= (LRRC51)	ENSP00000437561.1:n.-309G=
ENST00000538413.5:c.-186G= (LRRC51)	ENSP00000438762.1:n.-186G=
NM_001145307.4:c.-309G= (LRTOMT)	NP_001138779.1:n.-309G=
NM_001145308.4:c.-491G= (LRTOMT)	NP_001138780.1:n.-491G=
NM_001145309.3:c.-712G= (LRTOMT)	NP_001138781.1:n.-712G=
NM_001145310.3:c.-712G= (LRTOMT)	NP_001138782.1:n.-712G=
NM_001205138.3:c.-226G= (LRTOMT)	NP_001192067.1:n.-226G=
NM_001271471.2:c.-309G= (LRTOMT)	NP_001258400.1:n.-309G=
NM_145309.5:c.-309G= (LRTOMT)	NP_660352.1:n.-309G=
NR_026886.3:n.386G= (LRTOMT)
XM_006718473.2:c.-186G= (LRTOMT)	XP_006718536.1:n.-186G=
NM_001318803.1:c.-266G= (LRTOMT)	NP_001305732.1:n.-266G=
NR_134858.1:n.386G= (LRTOMT)
XM_006718473.4:c.-186G= (LRTOMT)	XP_006718536.1:n.-186G=
XM_006718474.4:c.-225G= (LRTOMT)	XP_006718537.1:n.-225G=
XM_011544848.3:c.-472G= (LRTOMT)	XP_011543150.1:n.-472G=