Canonical Allele Identifier: CA1149191491
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535330T= , CM000663.2:g.1535330T= GRCh38
NC_000001.10:g.1470710T= , CM000663.1:g.1470710T= GRCh37
NC_000001.9:g.1460573T= NCBI36
NG_041807.1:g.10031A=
NG_053035.1:g.28188T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*29A= MANE Select ENSP00000368007.4:n.*29A=
ENST00000378733.8:c.*29A= ENSP00000368007.4:n.*29A=
ENST00000425828.1:c.*29A= ENSP00000400311.1:n.*29A=
NM_001114748.1:c.*29A= NP_001108220.1:n.*29A=
NM_001114748.2:c.*29A= MANE Select NP_001108220.1:n.*29A=