Canonical Allele Identifier: CA415768596

Gene: TMEM240

Linked Data

• MyVariant Identifiers: chr1:g.1471009C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1535629C>G , CM000663.2:g.1535629C>G	GRCh38
NC_000001.10:g.1471009C>G , CM000663.1:g.1471009C>G	GRCh37
NC_000001.9:g.1460872C>G	NCBI36
NG_041807.1:g.9732G>C
NG_053035.1:g.28487C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378733.9:c.333G>C MANE Select	ENSP00000368007.4:p.Leu111=
ENST00000378733.8:c.333G>C	ENSP00000368007.4:p.Leu111=
ENST00000425828.1:c.333G>C	ENSP00000400311.1:p.Leu111=
NM_001114748.1:c.333G>C	NP_001108220.1:p.Leu111=
NM_001114748.2:c.333G>C MANE Select	NP_001108220.1:p.Leu111=