Canonical Allele Identifier: CA337866871

Gene: TMEM240

Linked Data

• gnomAD v4: 1-1535698-G-C
• MyVariant Identifiers: chr1:g.1471078G>C (hg19) ; chr1:g.1535698G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1535698G>C , CM000663.2:g.1535698G>C	GRCh38
NC_000001.10:g.1471078G>C , CM000663.1:g.1471078G>C	GRCh37
NC_000001.9:g.1460941G>C	NCBI36
NG_041807.1:g.9663C>G
NG_053035.1:g.28556G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378733.9:c.264C>G MANE Select	ENSP00000368007.4:p.Ile88Met
ENST00000378733.8:c.264C>G	ENSP00000368007.4:p.Ile88Met
ENST00000425828.1:c.264C>G	ENSP00000400311.1:p.Ile88Met
NM_001114748.1:c.264C>G	NP_001108220.1:p.Ile88Met
NM_001114748.2:c.264C>G MANE Select	NP_001108220.1:p.Ile88Met