Canonical Allele Identifier: CA1694169910

Gene: TOMM7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22817012_22817013delinsTA , CM000669.2:g.22817012_22817013delinsTA	GRCh38
NC_000007.13:g.22856631_22856632delinsTA , CM000669.1:g.22856631_22856632delinsTA	GRCh37
NC_000007.12:g.22823156_22823157delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+987_152+988delinsTA MANE Select	ENSP00000351214.4:n.152+987_152+988delinsTA
ENST00000358435.8:c.152+987_152+988delinsTA	ENSP00000351214.4:n.152+987_152+988delinsTA
ENST00000372879.8:c.289+399_289+400delinsTA	ENSP00000361970.4:n.289+399_289+400delinsTA
ENST00000405021.7:c.140+987_140+988delinsTA	ENSP00000385203.3:n.140+987_140+988delinsTA
ENST00000463284.2:n.174-3828_174-3827delinsTA
ENST00000483581.1:n.336+987_336+988delinsTA
NM_019059.3:c.152+987_152+988delinsTA	NP_061932.1:n.152+987_152+988delinsTA
NM_019059.4:c.152+987_152+988delinsTA	NP_061932.1:n.152+987_152+988delinsTA
NM_019059.5:c.152+987_152+988delinsTA MANE Select	NP_061932.1:n.152+987_152+988delinsTA
NR_168014.1:n.178+987_178+988delinsTA
NR_168015.1:n.130-3828_130-3827delinsTA