Canonical Allele Identifier: CA357064449
Gene: TMPRSS11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68797741T>G (hg19) chr4:g.67932023T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932023T>G , CM000666.2:g.67932023T>G GRCh38
NC_000004.11:g.68797741T>G , CM000666.1:g.68797741T>G GRCh37
NC_000004.10:g.68480336T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.290A>C MANE Select ENSP00000426911.2:p.Asn97Thr
ENST00000334830.11:c.299A>C ENSP00000334611.7:p.Asn100Thr
ENST00000396188.3:c.290A>C ENSP00000379491.3:p.Asn97Thr
ENST00000508048.5:c.290A>C ENSP00000426911.2:p.Asn97Thr
ENST00000513536.5:c.230A>C ENSP00000427621.1:p.Asn77Thr
NM_001114387.1:c.290A>C NP_001107859.1:p.Asn97Thr
NM_182606.3:c.299A>C NP_872412.3:p.Asn100Thr
NM_001114387.2:c.290A>C MANE Select NP_001107859.1:p.Asn97Thr
NM_182606.4:c.299A>C NP_872412.3:p.Asn100Thr
Search 100 bp 5'
Search 100 bp 3'