Canonical Allele Identifier: CA1149192900
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535713C= , CM000663.2:g.1535713C= GRCh38
NC_000001.10:g.1471093C= , CM000663.1:g.1471093C= GRCh37
NC_000001.9:g.1460956C= NCBI36
NG_041807.1:g.9648G=
NG_053035.1:g.28571C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.249G= MANE Select ENSP00000368007.4:p.Val83=
ENST00000378733.8:c.249G= ENSP00000368007.4:p.Val83=
ENST00000425828.1:c.249G= ENSP00000400311.1:p.Val83=
NM_001114748.1:c.249G= NP_001108220.1:p.Val83=
NM_001114748.2:c.249G= MANE Select NP_001108220.1:p.Val83=