Canonical Allele Identifier: CA889464940
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1290820008
gnomAD v3: 1-1535855-C-CG
gnomAD v4: 1-1535855-C-CG
MyVariant Identifiers: chr1:g.1471235_1471236insG (hg19) chr1:g.1535855_1535856insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535859dup , CM000663.2:g.1535859dup GRCh38
NC_000001.10:g.1471239dup , CM000663.1:g.1471239dup GRCh37
NC_000001.9:g.1461102dup NCBI36
NG_041807.1:g.9505dup
NG_053035.1:g.28717dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.165-59dup MANE Select ENSP00000368007.4:n.165-59dup
ENST00000378733.8:c.165-59dup ENSP00000368007.4:n.165-59dup
ENST00000425828.1:c.165-59dup ENSP00000400311.1:n.165-59dup
NM_001114748.1:c.165-59dup NP_001108220.1:n.165-59dup
NM_001114748.2:c.165-59dup MANE Select NP_001108220.1:n.165-59dup
Search 100 bp 5'
Search 100 bp 3'