Canonical Allele Identifier: CA1465503920
Gene: TMPRSS11A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932256T= , CM000666.2:g.67932256T= GRCh38
NC_000004.11:g.68797974T= , CM000666.1:g.68797974T= GRCh37
NC_000004.10:g.68480569T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.253-196A= MANE Select ENSP00000426911.2:n.253-196A=
ENST00000334830.11:c.262-196A= ENSP00000334611.7:n.262-196A=
ENST00000396188.3:c.253-196A= ENSP00000379491.3:n.253-196A=
ENST00000508048.5:c.253-196A= ENSP00000426911.2:n.253-196A=
ENST00000513536.5:c.193-196A= ENSP00000427621.1:n.193-196A=
NM_001114387.1:c.253-196A= NP_001107859.1:n.253-196A=
NM_182606.3:c.262-196A= NP_872412.3:n.262-196A=
NM_001114387.2:c.253-196A= MANE Select NP_001107859.1:n.253-196A=
NM_182606.4:c.262-196A= NP_872412.3:n.262-196A=
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