Canonical Allele Identifier: CA600079855

Gene: LRRC51 NUMA1 LRTOMT

Linked Data

• dbSNP Id: rs1244124733
• gnomAD v2: 11-71791700-G-A
• gnomAD v3: 11-72080654-G-A
• gnomAD v4: 11-72080654-G-A
• MyVariant Identifiers: chr11:g.71791700G>A (hg19) ; chr11:g.72080654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72080654G>A , CM000673.2:g.72080654G>A	GRCh38
NC_000011.9:g.71791700G>A , CM000673.1:g.71791700G>A	GRCh37
NC_000011.8:g.71469348G>A	NCBI36
NG_021423.1:g.5319G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289488.7:c.-371G>A (LRRC51)	ENSP00000289488.2:n.-371G>A
ENST00000535883.6:c.-248G>A (LRRC51)	ENSP00000437561.1:n.-248G>A
ENST00000538413.6:c.-287G>A (LRRC51)	ENSP00000438762.2:n.-287G>A
ENST00000539271.6:c.-441G>A (LRRC51)	ENSP00000442267.2:n.-441G>A
ENST00000642648.1:c.-248G>A (LRRC51)	ENSP00000494362.1:n.-248G>A
ENST00000642813.1:n.89G>A (LRRC51)
ENST00000647530.1:c.-534G>A (LRRC51)	ENSP00000494072.1:n.-534G>A
ENST00000289488.6:c.-371G>A (LRRC51)	ENSP00000289488.2:n.-371G>A
ENST00000307198.11:c.-553G>A (LRRC51)	ENSP00000305742.7:n.-553G>A
ENST00000393695.7:c.-299C>T (NUMA1)	ENSP00000377298.3:n.-299C>T
ENST00000535883.5:c.-371G>A (LRRC51)	ENSP00000437561.1:n.-371G>A
ENST00000538413.5:c.-248G>A (LRRC51)	ENSP00000438762.1:n.-248G>A
ENST00000543450.1:n.40C>T (NUMA1)
ENST00000613205.4:c.-299C>T (NUMA1)	ENSP00000480172.1:n.-299C>T
NM_001145307.4:c.-371G>A (LRTOMT)	NP_001138779.1:n.-371G>A
NM_001145308.4:c.-553G>A (LRTOMT)	NP_001138780.1:n.-553G>A
NM_001145309.3:c.-774G>A (LRTOMT)	NP_001138781.1:n.-774G>A
NM_001145310.3:c.-774G>A (LRTOMT)	NP_001138782.1:n.-774G>A
NM_001205138.3:c.-288G>A (LRTOMT)	NP_001192067.1:n.-288G>A
NM_001271471.2:c.-371G>A (LRTOMT)	NP_001258400.1:n.-371G>A
NM_001286561.1:c.-397C>T (NUMA1)	NP_001273490.1:n.-397C>T
NM_006185.3:c.-299C>T (NUMA1)	NP_006176.2:n.-299C>T
NM_145309.5:c.-371G>A (LRTOMT)	NP_660352.1:n.-371G>A
NR_026886.3:n.324G>A (LRTOMT)
XM_011545055.1:c.-299C>T (NUMA1)	XP_011543357.1:n.-299C>T
NM_001318803.1:c.-328G>A (LRTOMT)	NP_001305732.1:n.-328G>A
NR_134858.1:n.324G>A (LRTOMT)
XM_006718474.4:c.-287G>A (LRTOMT)	XP_006718537.1:n.-287G>A
XM_011544848.3:c.-534G>A (LRTOMT)	XP_011543150.1:n.-534G>A