Canonical Allele Identifier: CA2670825661
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67931936-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931936T>C , CM000666.2:g.67931936T>C GRCh38
NC_000004.11:g.68797654T>C , CM000666.1:g.68797654T>C GRCh37
NC_000004.10:g.68480249T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320+57A>G MANE Select ENSP00000426911.2:n.320+57A>G
ENST00000334830.11:c.329+57A>G ENSP00000334611.7:n.329+57A>G
ENST00000396188.3:c.320+57A>G ENSP00000379491.3:n.320+57A>G
ENST00000508048.5:c.320+57A>G ENSP00000426911.2:n.320+57A>G
ENST00000513536.5:c.260+57A>G ENSP00000427621.1:n.260+57A>G
NM_001114387.1:c.320+57A>G NP_001107859.1:n.320+57A>G
NM_182606.3:c.329+57A>G NP_872412.3:n.329+57A>G
NM_001114387.2:c.320+57A>G MANE Select NP_001107859.1:n.320+57A>G
NM_182606.4:c.329+57A>G NP_872412.3:n.329+57A>G
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