Canonical Allele Identifier: CA2939716
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs745890637
gnomAD v2: 4-68797726-T-A
gnomAD v3: 4-67932008-T-A
gnomAD v4: 4-67932008-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932008T>A , CM000666.2:g.67932008T>A GRCh38
NC_000004.11:g.68797726T>A , CM000666.1:g.68797726T>A GRCh37
NC_000004.10:g.68480321T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.305A>T MANE Select ENSP00000426911.2:p.Gln102Leu
ENST00000334830.11:c.314A>T ENSP00000334611.7:p.Gln105Leu
ENST00000396188.3:c.305A>T ENSP00000379491.3:p.Gln102Leu
ENST00000508048.5:c.305A>T ENSP00000426911.2:p.Gln102Leu
ENST00000513536.5:c.245A>T ENSP00000427621.1:p.Gln82Leu
NM_001114387.1:c.305A>T NP_001107859.1:p.Gln102Leu
NM_182606.3:c.314A>T NP_872412.3:p.Gln105Leu
NM_001114387.2:c.305A>T MANE Select NP_001107859.1:p.Gln102Leu
NM_182606.4:c.314A>T NP_872412.3:p.Gln105Leu