Canonical Allele Identifier: CA600242563

Gene: LRTOMT LRRC51

Linked Data

• dbSNP Id: rs1304671899
• gnomAD v2: 11-71816961-C-T
• gnomAD v4: 11-72105915-C-T
• MyVariant Identifiers: chr11:g.71816961C>T (hg19) ; chr11:g.72105915C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72105915C>T , CM000673.2:g.72105915C>T	GRCh38
NC_000011.9:g.71816961C>T , CM000673.1:g.71816961C>T	GRCh37
NC_000011.8:g.71494609C>T	NCBI36
NG_021423.1:g.30580C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643715.1:c.438-2690C>T (LRTOMT)	ENSP00000496019.1:n.438-2690C>T
ENST00000646163.1:c.73-141C>T (LRTOMT)	ENSP00000494749.1:n.73-141C>T
ENST00000307198.11:c.84-21C>T (LRRC51)	ENSP00000305742.7:n.84-21C>T
ENST00000419228.2:c.84-141C>T (LRRC51)	ENSP00000392233.2:n.84-141C>T
ENST00000427369.6:c.487-21C>T (LRRC51)	ENSP00000409403.2:n.487-21C>T
ENST00000435085.5:c.84-21C>T (LRRC51)	ENSP00000409789.1:n.84-21C>T
ENST00000439209.5:c.438-2690C>T (LRRC51)	ENSP00000395139.1:n.438-2690C>T
ENST00000541899.1:n.121C>T (LRRC51)
ENST00000544409.5:c.487-141C>T (LRRC51)	ENSP00000440969.1:n.487-141C>T
NM_001145308.4:c.84-21C>T (LRTOMT)	NP_001138780.1:n.84-21C>T
NM_001145309.3:c.84-21C>T (LRTOMT)	NP_001138781.1:n.84-21C>T
NM_001145310.3:c.84-141C>T (LRTOMT)	NP_001138782.1:n.84-141C>T
XM_011544849.1:c.309-21C>T (LRTOMT)	XP_011543151.1:n.309-21C>T
XM_024448401.1:c.309-21C>T (LRTOMT)	XP_024304169.1:n.309-21C>T
NM_001145308.5:c.84-21C>T (LRTOMT)	NP_001138780.1:n.84-21C>T
NM_001145309.4:c.84-21C>T (LRTOMT)	NP_001138781.1:n.84-21C>T
NM_001145310.4:c.84-141C>T (LRTOMT)	NP_001138782.1:n.84-141C>T