Canonical Allele Identifier: CA337866638
Gene: TMEM240 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535655A>C , CM000663.2:g.1535655A>C GRCh38
NC_000001.10:g.1471035A>C , CM000663.1:g.1471035A>C GRCh37
NC_000001.9:g.1460898A>C NCBI36
NG_041807.1:g.9706T>G
NG_053035.1:g.28513A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.307T>G MANE Select ENSP00000368007.4:p.Phe103Val
ENST00000378733.8:c.307T>G ENSP00000368007.4:p.Phe103Val
ENST00000425828.1:c.307T>G ENSP00000400311.1:p.Phe103Val
NM_001114748.1:c.307T>G NP_001108220.1:p.Phe103Val
NM_001114748.2:c.307T>G MANE Select NP_001108220.1:p.Phe103Val