Canonical Allele Identifier: CA1149192956
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535729A= , CM000663.2:g.1535729A= GRCh38
NC_000001.10:g.1471109A= , CM000663.1:g.1471109A= GRCh37
NC_000001.9:g.1460972A= NCBI36
NG_041807.1:g.9632T=
NG_053035.1:g.28587A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.233T= MANE Select ENSP00000368007.4:p.Phe78=
ENST00000378733.8:c.233T= ENSP00000368007.4:p.Phe78=
ENST00000425828.1:c.233T= ENSP00000400311.1:p.Phe78=
NM_001114748.1:c.233T= NP_001108220.1:p.Phe78=
NM_001114748.2:c.233T= MANE Select NP_001108220.1:p.Phe78=