Canonical Allele Identifier: CA337865968
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1470819A>T (hg19) chr1:g.1535439A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535439A>T , CM000663.2:g.1535439A>T GRCh38
NC_000001.10:g.1470819A>T , CM000663.1:g.1470819A>T GRCh37
NC_000001.9:g.1460682A>T NCBI36
NG_041807.1:g.9922T>A
NG_053035.1:g.28297A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.442T>A MANE Select ENSP00000368007.4:p.Phe148Ile
ENST00000378733.8:c.442T>A ENSP00000368007.4:p.Phe148Ile
ENST00000425828.1:c.442T>A ENSP00000400311.1:p.Phe148Ile
NM_001114748.1:c.442T>A NP_001108220.1:p.Phe148Ile
NM_001114748.2:c.442T>A MANE Select NP_001108220.1:p.Phe148Ile
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