Canonical Allele Identifier: CA337866419
Gene: TMEM240 HGNC NCBI

Linked Data

gnomAD v4: 1-1535616-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535616G>T , CM000663.2:g.1535616G>T GRCh38
NC_000001.10:g.1470996G>T , CM000663.1:g.1470996G>T GRCh37
NC_000001.9:g.1460859G>T NCBI36
NG_041807.1:g.9745C>A
NG_053035.1:g.28474G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.346C>A MANE Select ENSP00000368007.4:p.Arg116Ser
ENST00000378733.8:c.346C>A ENSP00000368007.4:p.Arg116Ser
ENST00000425828.1:c.346C>A ENSP00000400311.1:p.Arg116Ser
NM_001114748.1:c.346C>A NP_001108220.1:p.Arg116Ser
NM_001114748.2:c.346C>A MANE Select NP_001108220.1:p.Arg116Ser