Canonical Allele Identifier: CA2670825747
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67932121-C-A

Genomic Alleles

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

Transcript Alleles

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