Canonical Allele Identifier: CA1149192474
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535577_1535580delinsCGAG , CM000663.2:g.1535577_1535580delinsCGAG GRCh38
NC_000001.10:g.1470957_1470960delinsCGAG , CM000663.1:g.1470957_1470960delinsCGAG GRCh37
NC_000001.9:g.1460820_1460823delinsCGAG NCBI36
NG_041807.1:g.9781_9784delinsCTCG
NG_053035.1:g.28435_28438delinsCGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.373+9_373+12delinsCTCG MANE Select ENSP00000368007.4:n.373+9_373+12delinsCTCG
ENST00000378733.8:c.373+9_373+12delinsCTCG ENSP00000368007.4:n.373+9_373+12delinsCTCG
ENST00000425828.1:c.373+9_373+12delinsCTCG ENSP00000400311.1:n.373+9_373+12delinsCTCG
NM_001114748.1:c.373+9_373+12delinsCTCG NP_001108220.1:n.373+9_373+12delinsCTCG
NM_001114748.2:c.373+9_373+12delinsCTCG MANE Select NP_001108220.1:n.373+9_373+12delinsCTCG