Canonical Allele Identifier: CA1149192103
Gene: TMEM240 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535486G= , CM000663.2:g.1535486G= GRCh38
NC_000001.10:g.1470866G= , CM000663.1:g.1470866G= GRCh37
NC_000001.9:g.1460729G= NCBI36
NG_041807.1:g.9875C=
NG_053035.1:g.28344G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.395C= MANE Select ENSP00000368007.4:p.Pro132=
ENST00000378733.8:c.395C= ENSP00000368007.4:p.Pro132=
ENST00000425828.1:c.395C= ENSP00000400311.1:p.Pro132=
NM_001114748.1:c.395C= NP_001108220.1:p.Pro132=
NM_001114748.2:c.395C= MANE Select NP_001108220.1:p.Pro132=
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