Canonical Allele Identifier: CA357064376
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67931993-G-T
MyVariant Identifiers: chr4:g.68797711G>T (hg19) chr4:g.67931993G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931993G>T , CM000666.2:g.67931993G>T GRCh38
NC_000004.11:g.68797711G>T , CM000666.1:g.68797711G>T GRCh37
NC_000004.10:g.68480306G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320C>A MANE Select ENSP00000426911.2:p.Thr107Asn
ENST00000334830.11:c.329C>A ENSP00000334611.7:p.Thr110Asn
ENST00000396188.3:c.320C>A ENSP00000379491.3:p.Thr107Asn
ENST00000508048.5:c.320C>A ENSP00000426911.2:p.Thr107Asn
ENST00000513536.5:c.260C>A ENSP00000427621.1:p.Thr87Asn
NM_001114387.1:c.320C>A NP_001107859.1:p.Thr107Asn
NM_182606.3:c.329C>A NP_872412.3:p.Thr110Asn
NM_001114387.2:c.320C>A MANE Select NP_001107859.1:p.Thr107Asn
NM_182606.4:c.329C>A NP_872412.3:p.Thr110Asn
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