Canonical Allele Identifier: CA337865798
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1470776A>C (hg19) chr1:g.1535396A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535396A>C , CM000663.2:g.1535396A>C GRCh38
NC_000001.10:g.1470776A>C , CM000663.1:g.1470776A>C GRCh37
NC_000001.9:g.1460639A>C NCBI36
NG_041807.1:g.9965T>G
NG_053035.1:g.28254A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.485T>G MANE Select ENSP00000368007.4:p.Leu162Arg
ENST00000378733.8:c.485T>G ENSP00000368007.4:p.Leu162Arg
ENST00000425828.1:c.485T>G ENSP00000400311.1:p.Leu162Arg
NM_001114748.1:c.485T>G NP_001108220.1:p.Leu162Arg
NM_001114748.2:c.485T>G MANE Select NP_001108220.1:p.Leu162Arg
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