Canonical Allele Identifier: CA415388155
Gene: TMEM240 HGNC NCBI

Linked Data

ClinVar Variation Id: 728099
ClinVar RCV Id: RCV000902521
dbSNP Id: rs1442872142
gnomAD v2: 1-1470832-C-T
gnomAD v3: 1-1535452-C-T
gnomAD v4: 1-1535452-C-T
MyVariant Identifiers: chr1:g.1470832C>T (hg19) chr1:g.1535452C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535452C>T , CM000663.2:g.1535452C>T GRCh38
NC_000001.10:g.1470832C>T , CM000663.1:g.1470832C>T GRCh37
NC_000001.9:g.1460695C>T NCBI36
NG_041807.1:g.9909G>A
NG_053035.1:g.28310C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.429G>A MANE Select ENSP00000368007.4:p.Arg143=
ENST00000378733.8:c.429G>A ENSP00000368007.4:p.Arg143=
ENST00000425828.1:c.429G>A ENSP00000400311.1:p.Arg143=
NM_001114748.1:c.429G>A NP_001108220.1:p.Arg143=
NM_001114748.2:c.429G>A MANE Select NP_001108220.1:p.Arg143=
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