Canonical Allele Identifier: CA1149191381
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1642194584
gnomAD v4: 1-1535273-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535273C>A , CM000663.2:g.1535273C>A GRCh38
NC_000001.10:g.1470653C>A , CM000663.1:g.1470653C>A GRCh37
NC_000001.9:g.1460516C>A NCBI36
NG_041807.1:g.10088G>T
NG_053035.1:g.28131C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*86G>T MANE Select ENSP00000368007.4:n.*86G>T
ENST00000378733.8:c.*86G>T ENSP00000368007.4:n.*86G>T
ENST00000425828.1:c.*86G>T ENSP00000400311.1:n.*86G>T
NM_001114748.1:c.*86G>T NP_001108220.1:n.*86G>T
NM_001114748.2:c.*86G>T MANE Select NP_001108220.1:n.*86G>T