Canonical Allele Identifier: CA889464293
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1205201782
gnomAD v3: 1-1535265-TGTC-T
gnomAD v4: 1-1535265-TGTC-T
MyVariant Identifiers: chr1:g.1470646_1470648del (hg19) chr1:g.1535266_1535268del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535266_1535268del , CM000663.2:g.1535266_1535268del GRCh38
NC_000001.10:g.1470646_1470648del , CM000663.1:g.1470646_1470648del GRCh37
NC_000001.9:g.1460509_1460511del NCBI36
NG_041807.1:g.10093_10095del
NG_053035.1:g.28124_28126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*91_*93del MANE Select ENSP00000368007.4:n.*91_*93del
ENST00000378733.8:c.*91_*93del ENSP00000368007.4:n.*91_*93del
ENST00000425828.1:c.*91_*93del ENSP00000400311.1:n.*91_*93del
NM_001114748.1:c.*91_*93del NP_001108220.1:n.*91_*93del
NM_001114748.2:c.*91_*93del MANE Select NP_001108220.1:n.*91_*93del
Search 100 bp 5'
Search 100 bp 3'