Canonical Allele Identifier: CA224380597

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs886048623
• gnomAD v2: 11-71791772-G-A
• gnomAD v3: 11-72080726-G-A
• gnomAD v4: 11-72080726-G-A
• MyVariant Identifiers: chr11:g.71791772G>A (hg19) ; chr11:g.72080726G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080726G>A , CM000673.2:g.72080726G>A	GRCh38
NC_000011.9:g.71791772G>A , CM000673.1:g.71791772G>A	GRCh37
NC_000011.8:g.71469420G>A	NCBI36
NG_021423.1:g.5391G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-299G>A (LRRC51)	ENSP00000289488.2:n.-299G>A
ENST00000535883.6:c.-176G>A (LRRC51)	ENSP00000437561.1:n.-176G>A
ENST00000538413.6:c.-215G>A (LRRC51)	ENSP00000438762.2:n.-215G>A
ENST00000539271.6:c.-369G>A (LRRC51)	ENSP00000442267.2:n.-369G>A
ENST00000642510.1:c.-492G>A (LRRC51)	ENSP00000496544.1:n.-492G>A
ENST00000642648.1:c.-176G>A (LRRC51)	ENSP00000494362.1:n.-176G>A
ENST00000642813.1:n.161G>A (LRRC51)
ENST00000647530.1:c.-462G>A (LRRC51)	ENSP00000494072.1:n.-462G>A
ENST00000289488.6:c.-299G>A (LRRC51)	ENSP00000289488.2:n.-299G>A
ENST00000307198.11:c.-481G>A (LRRC51)	ENSP00000305742.7:n.-481G>A
ENST00000535883.5:c.-299G>A (LRRC51)	ENSP00000437561.1:n.-299G>A
ENST00000538413.5:c.-176G>A (LRRC51)	ENSP00000438762.1:n.-176G>A
NM_001145307.4:c.-299G>A (LRTOMT)	NP_001138779.1:n.-299G>A
NM_001145308.4:c.-481G>A (LRTOMT)	NP_001138780.1:n.-481G>A
NM_001145309.3:c.-702G>A (LRTOMT)	NP_001138781.1:n.-702G>A
NM_001145310.3:c.-702G>A (LRTOMT)	NP_001138782.1:n.-702G>A
NM_001205138.3:c.-216G>A (LRTOMT)	NP_001192067.1:n.-216G>A
NM_001271471.2:c.-299G>A (LRTOMT)	NP_001258400.1:n.-299G>A
NM_145309.5:c.-299G>A (LRTOMT)	NP_660352.1:n.-299G>A
NR_026886.3:n.396G>A (LRTOMT)
XM_006718473.2:c.-176G>A (LRTOMT)	XP_006718536.1:n.-176G>A
NM_001318803.1:c.-256G>A (LRTOMT)	NP_001305732.1:n.-256G>A
NR_134858.1:n.396G>A (LRTOMT)
XM_006718473.4:c.-176G>A (LRTOMT)	XP_006718536.1:n.-176G>A
XM_006718474.4:c.-215G>A (LRTOMT)	XP_006718537.1:n.-215G>A
XM_011544848.3:c.-462G>A (LRTOMT)	XP_011543150.1:n.-462G>A