Canonical Allele Identifier: CA224380593

Gene: LRRC51 LRTOMT

Linked Data

• dbSNP Id: rs770538591
• gnomAD v4: 11-72080716-G-A
• MyVariant Identifiers: chr11:g.71791762G>A (hg19) ; chr11:g.72080716G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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