Canonical Allele Identifier: CA836784237

Gene: TOMM7

Linked Data

• dbSNP Id: rs1213268351
• MyVariant Identifiers: chr7:g.22856679_22856680insGACAG (hg19) ; chr7:g.22817060_22817061insGACAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22817062_22817063insCAGGA , CM000669.2:g.22817062_22817063insCAGGA	GRCh38
NC_000007.13:g.22856681_22856682insCAGGA , CM000669.1:g.22856681_22856682insCAGGA	GRCh37
NC_000007.12:g.22823206_22823207insCAGGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358435.9:c.152+939_152+940insCTGTC MANE Select	ENSP00000351214.4:n.152+939_152+940insCTGTC
ENST00000358435.8:c.152+939_152+940insCTGTC	ENSP00000351214.4:n.152+939_152+940insCTGTC
ENST00000372879.8:c.289+351_289+352insCTGTC	ENSP00000361970.4:n.289+351_289+352insCTGTC
ENST00000405021.7:c.140+939_140+940insCTGTC	ENSP00000385203.3:n.140+939_140+940insCTGTC
ENST00000463284.2:n.174-3876_174-3875insCTGTC
ENST00000483581.1:n.336+939_336+940insCTGTC
NM_019059.3:c.152+939_152+940insCTGTC	NP_061932.1:n.152+939_152+940insCTGTC
NM_019059.4:c.152+939_152+940insCTGTC	NP_061932.1:n.152+939_152+940insCTGTC
NM_019059.5:c.152+939_152+940insCTGTC MANE Select	NP_061932.1:n.152+939_152+940insCTGTC
NR_168014.1:n.178+939_178+940insCTGTC
NR_168015.1:n.130-3876_130-3875insCTGTC