Canonical Allele Identifier: CA415388117
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1470757G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535377G>A , CM000663.2:g.1535377G>A GRCh38
NC_000001.10:g.1470757G>A , CM000663.1:g.1470757G>A GRCh37
NC_000001.9:g.1460620G>A NCBI36
NG_041807.1:g.9984C>T
NG_053035.1:g.28235G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.504C>T MANE Select ENSP00000368007.4:p.Pro168=
ENST00000378733.8:c.504C>T ENSP00000368007.4:p.Pro168=
ENST00000425828.1:c.504C>T ENSP00000400311.1:p.Pro168=
NM_001114748.1:c.504C>T NP_001108220.1:p.Pro168=
NM_001114748.2:c.504C>T MANE Select NP_001108220.1:p.Pro168=
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