Canonical Allele Identifier: CA2939705
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs747531061
ExAC: 4:68797668 TC / T
gnomAD v2: 4-68797668-TC-T
gnomAD v3: 4-67931950-TC-T
gnomAD v4: 4-67931950-TC-T
MyVariant Identifiers: chr4:g.68797669del (hg19) chr4:g.67931951del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931953del , CM000666.2:g.67931953del GRCh38
NC_000004.11:g.68797671del , CM000666.1:g.68797671del GRCh37
NC_000004.10:g.68480266del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320+42del MANE Select ENSP00000426911.2:n.320+42del
ENST00000334830.11:c.329+42del ENSP00000334611.7:n.329+42del
ENST00000396188.3:c.320+42del ENSP00000379491.3:n.320+42del
ENST00000508048.5:c.320+42del ENSP00000426911.2:n.320+42del
ENST00000513536.5:c.260+42del ENSP00000427621.1:n.260+42del
NM_001114387.1:c.320+42del NP_001107859.1:n.320+42del
NM_182606.3:c.329+42del NP_872412.3:n.329+42del
NM_001114387.2:c.320+42del MANE Select NP_001107859.1:n.320+42del
NM_182606.4:c.329+42del NP_872412.3:n.329+42del
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