Canonical Allele Identifier: CA1149191530
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535341G= , CM000663.2:g.1535341G= GRCh38
NC_000001.10:g.1470721G= , CM000663.1:g.1470721G= GRCh37
NC_000001.9:g.1460584G= NCBI36
NG_041807.1:g.10020C=
NG_053035.1:g.28199G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*18C= MANE Select ENSP00000368007.4:n.*18C=
ENST00000378733.8:c.*18C= ENSP00000368007.4:n.*18C=
ENST00000425828.1:c.*18C= ENSP00000400311.1:n.*18C=
NM_001114748.1:c.*18C= NP_001108220.1:n.*18C=
NM_001114748.2:c.*18C= MANE Select NP_001108220.1:n.*18C=