Canonical Allele Identifier: CA2706083418
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs2109750058

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932135A>T , CM000666.2:g.67932135A>T GRCh38
NC_000004.11:g.68797853A>T , CM000666.1:g.68797853A>T GRCh37
NC_000004.10:g.68480448A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.253-75T>A MANE Select ENSP00000426911.2:n.253-75T>A
ENST00000334830.11:c.262-75T>A ENSP00000334611.7:n.262-75T>A
ENST00000396188.3:c.253-75T>A ENSP00000379491.3:n.253-75T>A
ENST00000508048.5:c.253-75T>A ENSP00000426911.2:n.253-75T>A
ENST00000513536.5:c.193-75T>A ENSP00000427621.1:n.193-75T>A
NM_001114387.1:c.253-75T>A NP_001107859.1:n.253-75T>A
NM_182606.3:c.262-75T>A NP_872412.3:n.262-75T>A
NM_001114387.2:c.253-75T>A MANE Select NP_001107859.1:n.253-75T>A
NM_182606.4:c.262-75T>A NP_872412.3:n.262-75T>A