Canonical Allele Identifier: CA337866392
Gene: TMEM240 HGNC NCBI

Linked Data

gnomAD v4: 1-1535610-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535610A>C , CM000663.2:g.1535610A>C GRCh38
NC_000001.10:g.1470990A>C , CM000663.1:g.1470990A>C GRCh37
NC_000001.9:g.1460853A>C NCBI36
NG_041807.1:g.9751T>G
NG_053035.1:g.28468A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.352T>G MANE Select ENSP00000368007.4:p.Trp118Gly
ENST00000378733.8:c.352T>G ENSP00000368007.4:p.Trp118Gly
ENST00000425828.1:c.352T>G ENSP00000400311.1:p.Trp118Gly
NM_001114748.1:c.352T>G NP_001108220.1:p.Trp118Gly
NM_001114748.2:c.352T>G MANE Select NP_001108220.1:p.Trp118Gly