Canonical Allele Identifier: CA1694169833

Gene: TOMM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22816939G= , CM000669.2:g.22816939G=	GRCh38
NC_000007.13:g.22856558G= , CM000669.1:g.22856558G=	GRCh37
NC_000007.12:g.22823083G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+1061C= MANE Select	ENSP00000351214.4:n.152+1061C=
ENST00000358435.8:c.152+1061C=	ENSP00000351214.4:n.152+1061C=
ENST00000372879.8:c.289+473C=	ENSP00000361970.4:n.289+473C=
ENST00000405021.7:c.140+1061C=	ENSP00000385203.3:n.140+1061C=
ENST00000463284.2:n.174-3754C=
ENST00000483581.1:n.336+1061C=
NM_019059.3:c.152+1061C=	NP_061932.1:n.152+1061C=
NM_019059.4:c.152+1061C=	NP_061932.1:n.152+1061C=
NM_019059.5:c.152+1061C= MANE Select	NP_061932.1:n.152+1061C=
NR_168014.1:n.178+1061C=
NR_168015.1:n.130-3754C=