Canonical Allele Identifier: CA1149193130
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535806G= , CM000663.2:g.1535806G= GRCh38
NC_000001.10:g.1471186G= , CM000663.1:g.1471186G= GRCh37
NC_000001.9:g.1461049G= NCBI36
NG_041807.1:g.9555C=
NG_053035.1:g.28664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.165-9C= MANE Select ENSP00000368007.4:n.165-9C=
ENST00000378733.8:c.165-9C= ENSP00000368007.4:n.165-9C=
ENST00000425828.1:c.165-9C= ENSP00000400311.1:n.165-9C=
NM_001114748.1:c.165-9C= NP_001108220.1:n.165-9C=
NM_001114748.2:c.165-9C= MANE Select NP_001108220.1:n.165-9C=