Canonical Allele Identifier: CA357064433
Gene: TMPRSS11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68797738T>G (hg19) chr4:g.67932020T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932020T>G , CM000666.2:g.67932020T>G GRCh38
NC_000004.11:g.68797738T>G , CM000666.1:g.68797738T>G GRCh37
NC_000004.10:g.68480333T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.293A>C MANE Select ENSP00000426911.2:p.Tyr98Ser
ENST00000334830.11:c.302A>C ENSP00000334611.7:p.Tyr101Ser
ENST00000396188.3:c.293A>C ENSP00000379491.3:p.Tyr98Ser
ENST00000508048.5:c.293A>C ENSP00000426911.2:p.Tyr98Ser
ENST00000513536.5:c.233A>C ENSP00000427621.1:p.Tyr78Ser
NM_001114387.1:c.293A>C NP_001107859.1:p.Tyr98Ser
NM_182606.3:c.302A>C NP_872412.3:p.Tyr101Ser
NM_001114387.2:c.293A>C MANE Select NP_001107859.1:p.Tyr98Ser
NM_182606.4:c.302A>C NP_872412.3:p.Tyr101Ser
Search 100 bp 5'
Search 100 bp 3'