Canonical Allele Identifier: CA357064500
Gene: TMPRSS11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68797753G>C (hg19) chr4:g.67932035G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932035G>C , CM000666.2:g.67932035G>C GRCh38
NC_000004.11:g.68797753G>C , CM000666.1:g.68797753G>C GRCh37
NC_000004.10:g.68480348G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.278C>G MANE Select ENSP00000426911.2:p.Ala93Gly
ENST00000334830.11:c.287C>G ENSP00000334611.7:p.Ala96Gly
ENST00000396188.3:c.278C>G ENSP00000379491.3:p.Ala93Gly
ENST00000508048.5:c.278C>G ENSP00000426911.2:p.Ala93Gly
ENST00000513536.5:c.218C>G ENSP00000427621.1:p.Ala73Gly
NM_001114387.1:c.278C>G NP_001107859.1:p.Ala93Gly
NM_182606.3:c.287C>G NP_872412.3:p.Ala96Gly
NM_001114387.2:c.278C>G MANE Select NP_001107859.1:p.Ala93Gly
NM_182606.4:c.287C>G NP_872412.3:p.Ala96Gly
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