Canonical Allele Identifier: CA357064488
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67932032-C-G
MyVariant Identifiers: chr4:g.68797750C>G (hg19) chr4:g.67932032C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932032C>G , CM000666.2:g.67932032C>G GRCh38
NC_000004.11:g.68797750C>G , CM000666.1:g.68797750C>G GRCh37
NC_000004.10:g.68480345C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.281G>C MANE Select ENSP00000426911.2:p.Trp94Ser
ENST00000334830.11:c.290G>C ENSP00000334611.7:p.Trp97Ser
ENST00000396188.3:c.281G>C ENSP00000379491.3:p.Trp94Ser
ENST00000508048.5:c.281G>C ENSP00000426911.2:p.Trp94Ser
ENST00000513536.5:c.221G>C ENSP00000427621.1:p.Trp74Ser
NM_001114387.1:c.281G>C NP_001107859.1:p.Trp94Ser
NM_182606.3:c.290G>C NP_872412.3:p.Trp97Ser
NM_001114387.2:c.281G>C MANE Select NP_001107859.1:p.Trp94Ser
NM_182606.4:c.290G>C NP_872412.3:p.Trp97Ser
Search 100 bp 5'
Search 100 bp 3'