Canonical Allele Identifier: CA1465503787
Gene: TMPRSS11A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932121C= , CM000666.2:g.67932121C= GRCh38
NC_000004.11:g.68797839C= , CM000666.1:g.68797839C= GRCh37
NC_000004.10:g.68480434C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.253-61G= MANE Select ENSP00000426911.2:n.253-61G=
ENST00000334830.11:c.262-61G= ENSP00000334611.7:n.262-61G=
ENST00000396188.3:c.253-61G= ENSP00000379491.3:n.253-61G=
ENST00000508048.5:c.253-61G= ENSP00000426911.2:n.253-61G=
ENST00000513536.5:c.193-61G= ENSP00000427621.1:n.193-61G=
NM_001114387.1:c.253-61G= NP_001107859.1:n.253-61G=
NM_182606.3:c.262-61G= NP_872412.3:n.262-61G=
NM_001114387.2:c.253-61G= MANE Select NP_001107859.1:n.253-61G=
NM_182606.4:c.262-61G= NP_872412.3:n.262-61G=
Search 100 bp 5'
Search 100 bp 3'