Canonical Allele Identifier: CA1144106778
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535855C= , CM000663.2:g.1535855C= GRCh38
NC_000001.10:g.1471235C= , CM000663.1:g.1471235C= GRCh37
NC_000001.9:g.1461098C= NCBI36
NG_041807.1:g.9506G=
NG_053035.1:g.28713C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.165-58G= MANE Select ENSP00000368007.4:n.165-58G=
ENST00000378733.8:c.165-58G= ENSP00000368007.4:n.165-58G=
ENST00000425828.1:c.165-58G= ENSP00000400311.1:n.165-58G=
NM_001114748.1:c.165-58G= NP_001108220.1:n.165-58G=
NM_001114748.2:c.165-58G= MANE Select NP_001108220.1:n.165-58G=