Canonical Allele Identifier: CA475864857

Gene: TOMT LRTOMT LRRC51

Linked Data

• gnomAD v4: 11-72106080-G-T
• MyVariant Identifiers: chr11:g.71817126G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72106080G>T , CM000673.2:g.72106080G>T	GRCh38
NC_000011.9:g.71817126G>T , CM000673.1:g.71817126G>T	GRCh37
NC_000011.8:g.71494774G>T	NCBI36
NG_021423.1:g.30745G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541899.3:c.129G>T (TOMT) MANE Select	ENSP00000494667.1:p.Leu43=
ENST00000541899.2:c.129G>T (TOMT)	ENSP00000494667.1:p.Leu43=
ENST00000643715.1:c.438-2525G>T (LRTOMT)	ENSP00000496019.1:n.438-2525G>T
ENST00000646163.1:c.97G>T (LRTOMT)	ENSP00000494749.1:p.Ala33Ser
ENST00000307198.11:c.228G>T (LRRC51)	ENSP00000305742.7:p.Leu76=
ENST00000419228.2:c.108G>T (LRRC51)	ENSP00000392233.2:p.Leu36=
ENST00000427369.6:c.631G>T (LRRC51)	ENSP00000409403.2:p.Ala211Ser
ENST00000435085.5:c.228G>T (LRRC51)	ENSP00000409789.1:p.Leu76=
ENST00000439209.5:c.438-2525G>T (LRRC51)	ENSP00000395139.1:n.438-2525G>T
ENST00000541899.1:n.286G>T (LRRC51)
ENST00000544409.5:c.511G>T (LRRC51)	ENSP00000440969.1:p.Ala171Ser
NM_001145308.4:c.228G>T (LRTOMT)	NP_001138780.1:p.Leu76=
NM_001145309.3:c.228G>T (LRTOMT)	NP_001138781.1:p.Leu76=
NM_001145310.3:c.108G>T (LRTOMT)	NP_001138782.1:p.Leu36=
XM_011544849.1:c.453G>T (LRTOMT)	XP_011543151.1:p.Leu151=
XM_024448401.1:c.453G>T (LRTOMT)	XP_024304169.1:p.Leu151=
NM_001145308.5:c.228G>T (LRTOMT)	NP_001138780.1:p.Leu76=
NM_001145309.4:c.228G>T (LRTOMT)	NP_001138781.1:p.Leu76=
NM_001145310.4:c.108G>T (LRTOMT)	NP_001138782.1:p.Leu36=
NM_001393500.1:c.129G>T (TOMT)	NP_001380429.1:p.Leu43=
NM_001393500.2:c.129G>T (TOMT) MANE Select	NP_001380429.1:p.Leu43=