Canonical Allele Identifier: CA679952858

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs1220550158
• MyVariant Identifiers: chr11:g.71791752A>C (hg19) ; chr11:g.72080706A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080706A>C , CM000673.2:g.72080706A>C	GRCh38
NC_000011.9:g.71791752A>C , CM000673.1:g.71791752A>C	GRCh37
NC_000011.8:g.71469400A>C	NCBI36
NG_021423.1:g.5371A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-319A>C (LRRC51)	ENSP00000289488.2:n.-319A>C
ENST00000535883.6:c.-196A>C (LRRC51)	ENSP00000437561.1:n.-196A>C
ENST00000538413.6:c.-235A>C (LRRC51)	ENSP00000438762.2:n.-235A>C
ENST00000539271.6:c.-389A>C (LRRC51)	ENSP00000442267.2:n.-389A>C
ENST00000642510.1:c.-512A>C (LRRC51)	ENSP00000496544.1:n.-512A>C
ENST00000642648.1:c.-196A>C (LRRC51)	ENSP00000494362.1:n.-196A>C
ENST00000642813.1:n.141A>C (LRRC51)
ENST00000647530.1:c.-482A>C (LRRC51)	ENSP00000494072.1:n.-482A>C
ENST00000289488.6:c.-319A>C (LRRC51)	ENSP00000289488.2:n.-319A>C
ENST00000307198.11:c.-501A>C (LRRC51)	ENSP00000305742.7:n.-501A>C
ENST00000535883.5:c.-319A>C (LRRC51)	ENSP00000437561.1:n.-319A>C
ENST00000538413.5:c.-196A>C (LRRC51)	ENSP00000438762.1:n.-196A>C
NM_001145307.4:c.-319A>C (LRTOMT)	NP_001138779.1:n.-319A>C
NM_001145308.4:c.-501A>C (LRTOMT)	NP_001138780.1:n.-501A>C
NM_001145309.3:c.-722A>C (LRTOMT)	NP_001138781.1:n.-722A>C
NM_001145310.3:c.-722A>C (LRTOMT)	NP_001138782.1:n.-722A>C
NM_001205138.3:c.-236A>C (LRTOMT)	NP_001192067.1:n.-236A>C
NM_001271471.2:c.-319A>C (LRTOMT)	NP_001258400.1:n.-319A>C
NM_145309.5:c.-319A>C (LRTOMT)	NP_660352.1:n.-319A>C
NR_026886.3:n.376A>C (LRTOMT)
XM_006718473.2:c.-196A>C (LRTOMT)	XP_006718536.1:n.-196A>C
NM_001318803.1:c.-276A>C (LRTOMT)	NP_001305732.1:n.-276A>C
NR_134858.1:n.376A>C (LRTOMT)
XM_006718473.4:c.-196A>C (LRTOMT)	XP_006718536.1:n.-196A>C
XM_006718474.4:c.-235A>C (LRTOMT)	XP_006718537.1:n.-235A>C
XM_011544848.3:c.-482A>C (LRTOMT)	XP_011543150.1:n.-482A>C