Canonical Allele Identifier: CA10631499

Gene: TOMT LRTOMT LRRC51 ANAPC15

Linked Data

• ClinVar Variation Id: 306003
• ClinVar RCV Id: RCV000301596
• dbSNP Id: rs886048636
• gnomAD v4: 11-72108921-G-A
• MyVariant Identifiers: chr11:g.71819967G>A (hg19) ; chr11:g.72108921G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72108921G>A , CM000673.2:g.72108921G>A	GRCh38
NC_000011.9:g.71819967G>A , CM000673.1:g.71819967G>A	GRCh37
NC_000011.8:g.71497615G>A	NCBI36
NG_021423.1:g.33586G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000541899.3:c.773G>A (TOMT) MANE Select	ENSP00000494667.1:p.Gly258Asp
ENST00000541899.2:c.773G>A (TOMT)	ENSP00000494667.1:p.Gly258Asp
ENST00000643715.1:c.*283G>A (LRTOMT)	ENSP00000496019.1:n.*283G>A
ENST00000307198.11:c.872G>A (LRRC51)	ENSP00000305742.7:p.Gly291Asp
ENST00000419228.2:c.*283G>A (LRRC51)	ENSP00000392233.2:n.*283G>A
ENST00000427369.6:c.*591G>A (LRRC51)	ENSP00000409403.2:n.*591G>A
ENST00000435085.5:c.872G>A (LRRC51)	ENSP00000409789.1:p.Gly291Asp
ENST00000502597.2:c.63+1167C>T (ANAPC15)	ENSP00000441774.1:n.63+1167C>T
ENST00000538117.5:c.*99-46C>T (ANAPC15)	ENSP00000445212.1:n.*99-46C>T
ENST00000543050.5:c.318+1167C>T (ANAPC15)	ENSP00000437360.1:n.318+1167C>T
ENST00000544409.5:c.*591G>A (LRRC51)	ENSP00000440969.1:n.*591G>A
NM_001145308.4:c.872G>A (LRTOMT)	NP_001138780.1:p.Gly291Asp
NM_001145309.3:c.872G>A (LRTOMT)	NP_001138781.1:p.Gly291Asp
NM_001145310.3:c.752G>A (LRTOMT)	NP_001138782.1:p.Gly251Asp
XM_011544849.1:c.1097G>A (LRTOMT)	XP_011543151.1:p.Gly366Asp
NM_001330321.1:c.318+1167C>T (ANAPC15)	NP_001317250.1:n.318+1167C>T
XM_024448401.1:c.1097G>A (LRTOMT)	XP_024304169.1:p.Gly366Asp
NM_001145308.5:c.872G>A (LRTOMT)	NP_001138780.1:p.Gly291Asp
NM_001145309.4:c.872G>A (LRTOMT)	NP_001138781.1:p.Gly291Asp
NM_001145310.4:c.752G>A (LRTOMT)	NP_001138782.1:p.Gly251Asp
NM_001330321.2:c.318+1167C>T (ANAPC15)	NP_001317250.1:n.318+1167C>T
NM_001393427.1:c.318+1167C>T (ANAPC15)	NP_001380356.1:n.318+1167C>T
NM_001393428.1:c.318+1167C>T (ANAPC15)	NP_001380357.1:n.318+1167C>T
NM_001393429.1:c.318+1167C>T (ANAPC15)	NP_001380358.1:n.318+1167C>T
NM_001393430.1:c.318+1167C>T (ANAPC15)	NP_001380359.1:n.318+1167C>T
NM_001393431.1:c.318+1167C>T (ANAPC15)	NP_001380360.1:n.318+1167C>T
NM_001393443.1:c.319-46C>T (ANAPC15)	NP_001380372.1:n.319-46C>T
NM_001393444.1:c.319-46C>T (ANAPC15)	NP_001380373.1:n.319-46C>T
NM_001393445.1:c.319-46C>T (ANAPC15)	NP_001380374.1:n.319-46C>T
NM_001393459.1:c.63+1167C>T (ANAPC15)	NP_001380388.1:n.63+1167C>T
NM_001393500.1:c.773G>A (TOMT)	NP_001380429.1:p.Gly258Asp
NR_171687.1:n.568-46C>T (ANAPC15)
NM_001393500.2:c.773G>A (TOMT) MANE Select	NP_001380429.1:p.Gly258Asp