Canonical Allele Identifier: CA552162435
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs1560567765

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932050_67932051dup , CM000666.2:g.67932050_67932051dup GRCh38
NC_000004.11:g.68797768_68797769dup , CM000666.1:g.68797768_68797769dup GRCh37
NC_000004.10:g.68480363_68480364dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.264_265dup MANE Select ENSP00000426911.2:p.Phe89TyrfsTer3
ENST00000334830.11:c.273_274dup ENSP00000334611.7:p.Phe92TyrfsTer3
ENST00000396188.3:c.264_265dup ENSP00000379491.3:p.Phe89TyrfsTer3
ENST00000508048.5:c.264_265dup ENSP00000426911.2:p.Phe89TyrfsTer3
ENST00000513536.5:c.204_205dup ENSP00000427621.1:p.Phe69TyrfsTer3
NM_001114387.1:c.264_265dup NP_001107859.1:p.Phe89TyrfsTer3
NM_182606.3:c.273_274dup NP_872412.3:p.Phe92TyrfsTer3
NM_001114387.2:c.264_265dup MANE Select NP_001107859.1:p.Phe89TyrfsTer3
NM_182606.4:c.273_274dup NP_872412.3:p.Phe92TyrfsTer3