Canonical Allele Identifier: CA357064428
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs1720637443
MyVariant Identifiers: chr4:g.68797736T>C (hg19) chr4:g.67932018T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932018T>C , CM000666.2:g.67932018T>C GRCh38
NC_000004.11:g.68797736T>C , CM000666.1:g.68797736T>C GRCh37
NC_000004.10:g.68480331T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.295A>G MANE Select ENSP00000426911.2:p.Ile99Val
ENST00000334830.11:c.304A>G ENSP00000334611.7:p.Ile102Val
ENST00000396188.3:c.295A>G ENSP00000379491.3:p.Ile99Val
ENST00000508048.5:c.295A>G ENSP00000426911.2:p.Ile99Val
ENST00000513536.5:c.235A>G ENSP00000427621.1:p.Ile79Val
NM_001114387.1:c.295A>G NP_001107859.1:p.Ile99Val
NM_182606.3:c.304A>G NP_872412.3:p.Ile102Val
NM_001114387.2:c.295A>G MANE Select NP_001107859.1:p.Ile99Val
NM_182606.4:c.304A>G NP_872412.3:p.Ile102Val
Search 100 bp 5'
Search 100 bp 3'