Canonical Allele Identifier: CA1694169885

Gene: TOMM7

Linked Data

• dbSNP Id: rs1583462983

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22816995A>T , CM000669.2:g.22816995A>T	GRCh38
NC_000007.13:g.22856614A>T , CM000669.1:g.22856614A>T	GRCh37
NC_000007.12:g.22823139A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+1005T>A MANE Select	ENSP00000351214.4:n.152+1005T>A
ENST00000358435.8:c.152+1005T>A	ENSP00000351214.4:n.152+1005T>A
ENST00000372879.8:c.289+417T>A	ENSP00000361970.4:n.289+417T>A
ENST00000405021.7:c.140+1005T>A	ENSP00000385203.3:n.140+1005T>A
ENST00000463284.2:n.174-3810T>A
ENST00000483581.1:n.336+1005T>A
NM_019059.3:c.152+1005T>A	NP_061932.1:n.152+1005T>A
NM_019059.4:c.152+1005T>A	NP_061932.1:n.152+1005T>A
NM_019059.5:c.152+1005T>A MANE Select	NP_061932.1:n.152+1005T>A
NR_168014.1:n.178+1005T>A
NR_168015.1:n.130-3810T>A