Canonical Allele Identifier: CA337865931
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1470812T>A (hg19) chr1:g.1535432T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535432T>A , CM000663.2:g.1535432T>A GRCh38
NC_000001.10:g.1470812T>A , CM000663.1:g.1470812T>A GRCh37
NC_000001.9:g.1460675T>A NCBI36
NG_041807.1:g.9929A>T
NG_053035.1:g.28290T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.449A>T MANE Select ENSP00000368007.4:p.Glu150Val
ENST00000378733.8:c.449A>T ENSP00000368007.4:p.Glu150Val
ENST00000425828.1:c.449A>T ENSP00000400311.1:p.Glu150Val
NM_001114748.1:c.449A>T NP_001108220.1:p.Glu150Val
NM_001114748.2:c.449A>T MANE Select NP_001108220.1:p.Glu150Val
Search 100 bp 5'
Search 100 bp 3'