Canonical Allele Identifier: CA415388181
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1470865G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535485G>A , CM000663.2:g.1535485G>A GRCh38
NC_000001.10:g.1470865G>A , CM000663.1:g.1470865G>A GRCh37
NC_000001.9:g.1460728G>A NCBI36
NG_041807.1:g.9876C>T
NG_053035.1:g.28343G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.396C>T MANE Select ENSP00000368007.4:p.Pro132=
ENST00000378733.8:c.396C>T ENSP00000368007.4:p.Pro132=
ENST00000425828.1:c.396C>T ENSP00000400311.1:p.Pro132=
NM_001114748.1:c.396C>T NP_001108220.1:p.Pro132=
NM_001114748.2:c.396C>T MANE Select NP_001108220.1:p.Pro132=
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