Canonical Allele Identifier: CA337866971
Gene: TMEM240 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535724T>A , CM000663.2:g.1535724T>A GRCh38
NC_000001.10:g.1471104T>A , CM000663.1:g.1471104T>A GRCh37
NC_000001.9:g.1460967T>A NCBI36
NG_041807.1:g.9637A>T
NG_053035.1:g.28582T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.238A>T MANE Select ENSP00000368007.4:p.Thr80Ser
ENST00000378733.8:c.238A>T ENSP00000368007.4:p.Thr80Ser
ENST00000425828.1:c.238A>T ENSP00000400311.1:p.Thr80Ser
NM_001114748.1:c.238A>T NP_001108220.1:p.Thr80Ser
NM_001114748.2:c.238A>T MANE Select NP_001108220.1:p.Thr80Ser