Canonical Allele Identifier: CA1694170019

Gene: TOMM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22817099A= , CM000669.2:g.22817099A=	GRCh38
NC_000007.13:g.22856718A= , CM000669.1:g.22856718A=	GRCh37
NC_000007.12:g.22823243A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+901T= MANE Select	ENSP00000351214.4:n.152+901T=
ENST00000358435.8:c.152+901T=	ENSP00000351214.4:n.152+901T=
ENST00000372879.8:c.289+313T=	ENSP00000361970.4:n.289+313T=
ENST00000405021.7:c.140+901T=	ENSP00000385203.3:n.140+901T=
ENST00000463284.2:n.174-3914T=
ENST00000483581.1:n.336+901T=
NM_019059.3:c.152+901T=	NP_061932.1:n.152+901T=
NM_019059.4:c.152+901T=	NP_061932.1:n.152+901T=
NM_019059.5:c.152+901T= MANE Select	NP_061932.1:n.152+901T=
NR_168014.1:n.178+901T=
NR_168015.1:n.130-3914T=