Canonical Allele Identifier: CA357064384
Gene: TMPRSS11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68797715G>C (hg19) chr4:g.67931997G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931997G>C , CM000666.2:g.67931997G>C GRCh38
NC_000004.11:g.68797715G>C , CM000666.1:g.68797715G>C GRCh37
NC_000004.10:g.68480310G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.316C>G MANE Select ENSP00000426911.2:p.Leu106Val
ENST00000334830.11:c.325C>G ENSP00000334611.7:p.Leu109Val
ENST00000396188.3:c.316C>G ENSP00000379491.3:p.Leu106Val
ENST00000508048.5:c.316C>G ENSP00000426911.2:p.Leu106Val
ENST00000513536.5:c.256C>G ENSP00000427621.1:p.Leu86Val
NM_001114387.1:c.316C>G NP_001107859.1:p.Leu106Val
NM_182606.3:c.325C>G NP_872412.3:p.Leu109Val
NM_001114387.2:c.316C>G MANE Select NP_001107859.1:p.Leu106Val
NM_182606.4:c.325C>G NP_872412.3:p.Leu109Val
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