Canonical Allele Identifier: CA98676615
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs529825761
gnomAD v3: 4-67931931-C-T
gnomAD v4: 4-67931931-C-T
MyVariant Identifiers: chr4:g.68797649C>T (hg19) chr4:g.67931931C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931931C>T , CM000666.2:g.67931931C>T GRCh38
NC_000004.11:g.68797649C>T , CM000666.1:g.68797649C>T GRCh37
NC_000004.10:g.68480244C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320+62G>A MANE Select ENSP00000426911.2:n.320+62G>A
ENST00000334830.11:c.329+62G>A ENSP00000334611.7:n.329+62G>A
ENST00000396188.3:c.320+62G>A ENSP00000379491.3:n.320+62G>A
ENST00000508048.5:c.320+62G>A ENSP00000426911.2:n.320+62G>A
ENST00000513536.5:c.260+62G>A ENSP00000427621.1:n.260+62G>A
NM_001114387.1:c.320+62G>A NP_001107859.1:n.320+62G>A
NM_182606.3:c.329+62G>A NP_872412.3:n.329+62G>A
NM_001114387.2:c.320+62G>A MANE Select NP_001107859.1:n.320+62G>A
NM_182606.4:c.329+62G>A NP_872412.3:n.329+62G>A
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