Canonical Allele Identifier: CA98676728
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs370242991
gnomAD v2: 4-68797727-G-T
gnomAD v3: 4-67932009-G-T
gnomAD v4: 4-67932009-G-T
COSMIC: COSM1328443
MyVariant Identifiers: chr4:g.68797727G>T (hg19) chr4:g.67932009G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932009G>T , CM000666.2:g.67932009G>T GRCh38
NC_000004.11:g.68797727G>T , CM000666.1:g.68797727G>T GRCh37
NC_000004.10:g.68480322G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.304C>A MANE Select ENSP00000426911.2:p.Gln102Lys
ENST00000334830.11:c.313C>A ENSP00000334611.7:p.Gln105Lys
ENST00000396188.3:c.304C>A ENSP00000379491.3:p.Gln102Lys
ENST00000508048.5:c.304C>A ENSP00000426911.2:p.Gln102Lys
ENST00000513536.5:c.244C>A ENSP00000427621.1:p.Gln82Lys
NM_001114387.1:c.304C>A NP_001107859.1:p.Gln102Lys
NM_182606.3:c.313C>A NP_872412.3:p.Gln105Lys
NM_001114387.2:c.304C>A MANE Select NP_001107859.1:p.Gln102Lys
NM_182606.4:c.313C>A NP_872412.3:p.Gln105Lys
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