Canonical Allele Identifier: CA224380584

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs528106946
• gnomAD v3: 11-72080711-C-G
• gnomAD v4: 11-72080711-C-G
• MyVariant Identifiers: chr11:g.71791757C>G (hg19) ; chr11:g.72080711C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080711C>G , CM000673.2:g.72080711C>G	GRCh38
NC_000011.9:g.71791757C>G , CM000673.1:g.71791757C>G	GRCh37
NC_000011.8:g.71469405C>G	NCBI36
NG_021423.1:g.5376C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-314C>G (LRRC51)	ENSP00000289488.2:n.-314C>G
ENST00000535883.6:c.-191C>G (LRRC51)	ENSP00000437561.1:n.-191C>G
ENST00000538413.6:c.-230C>G (LRRC51)	ENSP00000438762.2:n.-230C>G
ENST00000539271.6:c.-384C>G (LRRC51)	ENSP00000442267.2:n.-384C>G
ENST00000642510.1:c.-507C>G (LRRC51)	ENSP00000496544.1:n.-507C>G
ENST00000642648.1:c.-191C>G (LRRC51)	ENSP00000494362.1:n.-191C>G
ENST00000642813.1:n.146C>G (LRRC51)
ENST00000647530.1:c.-477C>G (LRRC51)	ENSP00000494072.1:n.-477C>G
ENST00000289488.6:c.-314C>G (LRRC51)	ENSP00000289488.2:n.-314C>G
ENST00000307198.11:c.-496C>G (LRRC51)	ENSP00000305742.7:n.-496C>G
ENST00000535883.5:c.-314C>G (LRRC51)	ENSP00000437561.1:n.-314C>G
ENST00000538413.5:c.-191C>G (LRRC51)	ENSP00000438762.1:n.-191C>G
NM_001145307.4:c.-314C>G (LRTOMT)	NP_001138779.1:n.-314C>G
NM_001145308.4:c.-496C>G (LRTOMT)	NP_001138780.1:n.-496C>G
NM_001145309.3:c.-717C>G (LRTOMT)	NP_001138781.1:n.-717C>G
NM_001145310.3:c.-717C>G (LRTOMT)	NP_001138782.1:n.-717C>G
NM_001205138.3:c.-231C>G (LRTOMT)	NP_001192067.1:n.-231C>G
NM_001271471.2:c.-314C>G (LRTOMT)	NP_001258400.1:n.-314C>G
NM_145309.5:c.-314C>G (LRTOMT)	NP_660352.1:n.-314C>G
NR_026886.3:n.381C>G (LRTOMT)
XM_006718473.2:c.-191C>G (LRTOMT)	XP_006718536.1:n.-191C>G
NM_001318803.1:c.-271C>G (LRTOMT)	NP_001305732.1:n.-271C>G
NR_134858.1:n.381C>G (LRTOMT)
XM_006718473.4:c.-191C>G (LRTOMT)	XP_006718536.1:n.-191C>G
XM_006718474.4:c.-230C>G (LRTOMT)	XP_006718537.1:n.-230C>G
XM_011544848.3:c.-477C>G (LRTOMT)	XP_011543150.1:n.-477C>G