Canonical Allele Identifier: CA2614916513

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• gnomAD v4: 11-72080691-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080691G>A , CM000673.2:g.72080691G>A	GRCh38
NC_000011.9:g.71791737G>A , CM000673.1:g.71791737G>A	GRCh37
NC_000011.8:g.71469385G>A	NCBI36
NG_021423.1:g.5356G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-334G>A (LRRC51)	ENSP00000289488.2:n.-334G>A
ENST00000535883.6:c.-211G>A (LRRC51)	ENSP00000437561.1:n.-211G>A
ENST00000538413.6:c.-250G>A (LRRC51)	ENSP00000438762.2:n.-250G>A
ENST00000539271.6:c.-404G>A (LRRC51)	ENSP00000442267.2:n.-404G>A
ENST00000642510.1:c.-527G>A (LRRC51)	ENSP00000496544.1:n.-527G>A
ENST00000642648.1:c.-211G>A (LRRC51)	ENSP00000494362.1:n.-211G>A
ENST00000642813.1:n.126G>A (LRRC51)
ENST00000647530.1:c.-497G>A (LRRC51)	ENSP00000494072.1:n.-497G>A
ENST00000289488.6:c.-334G>A (LRRC51)	ENSP00000289488.2:n.-334G>A
ENST00000307198.11:c.-516G>A (LRRC51)	ENSP00000305742.7:n.-516G>A
ENST00000535883.5:c.-334G>A (LRRC51)	ENSP00000437561.1:n.-334G>A
ENST00000538413.5:c.-211G>A (LRRC51)	ENSP00000438762.1:n.-211G>A
ENST00000543450.1:n.3C>T (NUMA1)
ENST00000613205.4:c.-336C>T (NUMA1)	ENSP00000480172.1:n.-336C>T
NM_001145307.4:c.-334G>A (LRTOMT)	NP_001138779.1:n.-334G>A
NM_001145308.4:c.-516G>A (LRTOMT)	NP_001138780.1:n.-516G>A
NM_001145309.3:c.-737G>A (LRTOMT)	NP_001138781.1:n.-737G>A
NM_001145310.3:c.-737G>A (LRTOMT)	NP_001138782.1:n.-737G>A
NM_001205138.3:c.-251G>A (LRTOMT)	NP_001192067.1:n.-251G>A
NM_001271471.2:c.-334G>A (LRTOMT)	NP_001258400.1:n.-334G>A
NM_001286561.1:c.-434C>T (NUMA1)	NP_001273490.1:n.-434C>T
NM_006185.3:c.-336C>T (NUMA1)	NP_006176.2:n.-336C>T
NM_145309.5:c.-334G>A (LRTOMT)	NP_660352.1:n.-334G>A
NR_026886.3:n.361G>A (LRTOMT)
XM_006718473.2:c.-211G>A (LRTOMT)	XP_006718536.1:n.-211G>A
NM_001318803.1:c.-291G>A (LRTOMT)	NP_001305732.1:n.-291G>A
NR_134858.1:n.361G>A (LRTOMT)
XM_006718473.4:c.-211G>A (LRTOMT)	XP_006718536.1:n.-211G>A
XM_006718474.4:c.-250G>A (LRTOMT)	XP_006718537.1:n.-250G>A
XM_011544848.3:c.-497G>A (LRTOMT)	XP_011543150.1:n.-497G>A