Canonical Allele Identifier: CA357064415
Gene: TMPRSS11A HGNC NCBI

Linked Data

COSMIC: COSM6100575
MyVariant Identifiers: chr4:g.68797731C>G (hg19) chr4:g.67932013C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932013C>G , CM000666.2:g.67932013C>G GRCh38
NC_000004.11:g.68797731C>G , CM000666.1:g.68797731C>G GRCh37
NC_000004.10:g.68480326C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.300G>C MANE Select ENSP00000426911.2:p.Lys100Asn
ENST00000334830.11:c.309G>C ENSP00000334611.7:p.Lys103Asn
ENST00000396188.3:c.300G>C ENSP00000379491.3:p.Lys100Asn
ENST00000508048.5:c.300G>C ENSP00000426911.2:p.Lys100Asn
ENST00000513536.5:c.240G>C ENSP00000427621.1:p.Lys80Asn
NM_001114387.1:c.300G>C NP_001107859.1:p.Lys100Asn
NM_182606.3:c.309G>C NP_872412.3:p.Lys103Asn
NM_001114387.2:c.300G>C MANE Select NP_001107859.1:p.Lys100Asn
NM_182606.4:c.309G>C NP_872412.3:p.Lys103Asn
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