Canonical Allele Identifier: CA1149191597
Gene: TMEM240 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535353T= , CM000663.2:g.1535353T= GRCh38
NC_000001.10:g.1470733T= , CM000663.1:g.1470733T= GRCh37
NC_000001.9:g.1460596T= NCBI36
NG_041807.1:g.10008A=
NG_053035.1:g.28211T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*6A= MANE Select ENSP00000368007.4:n.*6A=
ENST00000378733.8:c.*6A= ENSP00000368007.4:n.*6A=
ENST00000425828.1:c.*6A= ENSP00000400311.1:n.*6A=
NM_001114748.1:c.*6A= NP_001108220.1:n.*6A=
NM_001114748.2:c.*6A= MANE Select NP_001108220.1:n.*6A=