Canonical Allele Identifier: CA2544558473

Gene: TOMM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22816904_22816905insTG , CM000669.2:g.22816904_22816905insTG	GRCh38
NC_000007.13:g.22856523_22856524insTG , CM000669.1:g.22856523_22856524insTG	GRCh37
NC_000007.12:g.22823048_22823049insTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+1095_152+1096insCA MANE Select	ENSP00000351214.4:n.152+1095_152+1096insCA
ENST00000358435.8:c.152+1095_152+1096insCA	ENSP00000351214.4:n.152+1095_152+1096insCA
ENST00000372879.8:c.289+507_289+508insCA	ENSP00000361970.4:n.289+507_289+508insCA
ENST00000405021.7:c.140+1095_140+1096insCA	ENSP00000385203.3:n.140+1095_140+1096insCA
ENST00000463284.2:n.174-3720_174-3719insCA
ENST00000483581.1:n.336+1095_336+1096insCA
NM_019059.3:c.152+1095_152+1096insCA	NP_061932.1:n.152+1095_152+1096insCA
NM_019059.4:c.152+1095_152+1096insCA	NP_061932.1:n.152+1095_152+1096insCA
NM_019059.5:c.152+1095_152+1096insCA MANE Select	NP_061932.1:n.152+1095_152+1096insCA
NR_168014.1:n.178+1095_178+1096insCA
NR_168015.1:n.130-3720_130-3719insCA