Canonical Allele Identifier: CA337865916
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1470809G>C (hg19) chr1:g.1535429G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535429G>C , CM000663.2:g.1535429G>C GRCh38
NC_000001.10:g.1470809G>C , CM000663.1:g.1470809G>C GRCh37
NC_000001.9:g.1460672G>C NCBI36
NG_041807.1:g.9932C>G
NG_053035.1:g.28287G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.452C>G MANE Select ENSP00000368007.4:p.Ala151Gly
ENST00000378733.8:c.452C>G ENSP00000368007.4:p.Ala151Gly
ENST00000425828.1:c.452C>G ENSP00000400311.1:p.Ala151Gly
NM_001114748.1:c.452C>G NP_001108220.1:p.Ala151Gly
NM_001114748.2:c.452C>G MANE Select NP_001108220.1:p.Ala151Gly
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