Canonical Allele Identifier: CA1149192038
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535469G= , CM000663.2:g.1535469G= GRCh38
NC_000001.10:g.1470849G= , CM000663.1:g.1470849G= GRCh37
NC_000001.9:g.1460712G= NCBI36
NG_041807.1:g.9892C=
NG_053035.1:g.28327G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.412C= MANE Select ENSP00000368007.4:p.Arg138=
ENST00000378733.8:c.412C= ENSP00000368007.4:p.Arg138=
ENST00000425828.1:c.412C= ENSP00000400311.1:p.Arg138=
NM_001114748.1:c.412C= NP_001108220.1:p.Arg138=
NM_001114748.2:c.412C= MANE Select NP_001108220.1:p.Arg138=