Canonical Allele Identifier: CA1149191431
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1642195051
gnomAD v4: 1-1535290-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535290C>T , CM000663.2:g.1535290C>T GRCh38
NC_000001.10:g.1470670C>T , CM000663.1:g.1470670C>T GRCh37
NC_000001.9:g.1460533C>T NCBI36
NG_041807.1:g.10071G>A
NG_053035.1:g.28148C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*69G>A MANE Select ENSP00000368007.4:n.*69G>A
ENST00000378733.8:c.*69G>A ENSP00000368007.4:n.*69G>A
ENST00000425828.1:c.*69G>A ENSP00000400311.1:n.*69G>A
NM_001114748.1:c.*69G>A NP_001108220.1:n.*69G>A
NM_001114748.2:c.*69G>A MANE Select NP_001108220.1:n.*69G>A