Canonical Allele Identifier: CA1149191358
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535261C= , CM000663.2:g.1535261C= GRCh38
NC_000001.10:g.1470641C= , CM000663.1:g.1470641C= GRCh37
NC_000001.9:g.1460504C= NCBI36
NG_041807.1:g.10100G=
NG_053035.1:g.28119C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*98G= MANE Select ENSP00000368007.4:n.*98G=
ENST00000378733.8:c.*98G= ENSP00000368007.4:n.*98G=
ENST00000425828.1:c.*98G= ENSP00000400311.1:n.*98G=
NM_001114748.1:c.*98G= NP_001108220.1:n.*98G=
NM_001114748.2:c.*98G= MANE Select NP_001108220.1:n.*98G=