Canonical Allele Identifier: CA889464315
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1292284729
MyVariant Identifiers: chr1:g.1470699A>T (hg19) chr1:g.1535319A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535319A>T , CM000663.2:g.1535319A>T GRCh38
NC_000001.10:g.1470699A>T , CM000663.1:g.1470699A>T GRCh37
NC_000001.9:g.1460562A>T NCBI36
NG_041807.1:g.10042T>A
NG_053035.1:g.28177A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*40T>A MANE Select ENSP00000368007.4:n.*40T>A
ENST00000378733.8:c.*40T>A ENSP00000368007.4:n.*40T>A
ENST00000425828.1:c.*40T>A ENSP00000400311.1:n.*40T>A
NM_001114748.1:c.*40T>A NP_001108220.1:n.*40T>A
NM_001114748.2:c.*40T>A MANE Select NP_001108220.1:n.*40T>A
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