Canonical Allele Identifier: CA1149193011
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535749C= , CM000663.2:g.1535749C= GRCh38
NC_000001.10:g.1471129C= , CM000663.1:g.1471129C= GRCh37
NC_000001.9:g.1460992C= NCBI36
NG_041807.1:g.9612G=
NG_053035.1:g.28607C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.213G= MANE Select ENSP00000368007.4:p.Val71=
ENST00000378733.8:c.213G= ENSP00000368007.4:p.Val71=
ENST00000425828.1:c.213G= ENSP00000400311.1:p.Val71=
NM_001114748.1:c.213G= NP_001108220.1:p.Val71=
NM_001114748.2:c.213G= MANE Select NP_001108220.1:p.Val71=