Canonical Allele Identifier: CA1465503909
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs1720645634

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932248G>A , CM000666.2:g.67932248G>A GRCh38
NC_000004.11:g.68797966G>A , CM000666.1:g.68797966G>A GRCh37
NC_000004.10:g.68480561G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.253-188C>T MANE Select ENSP00000426911.2:n.253-188C>T
ENST00000334830.11:c.262-188C>T ENSP00000334611.7:n.262-188C>T
ENST00000396188.3:c.253-188C>T ENSP00000379491.3:n.253-188C>T
ENST00000508048.5:c.253-188C>T ENSP00000426911.2:n.253-188C>T
ENST00000513536.5:c.193-188C>T ENSP00000427621.1:n.193-188C>T
NM_001114387.1:c.253-188C>T NP_001107859.1:n.253-188C>T
NM_182606.3:c.262-188C>T NP_872412.3:n.262-188C>T
NM_001114387.2:c.253-188C>T MANE Select NP_001107859.1:n.253-188C>T
NM_182606.4:c.262-188C>T NP_872412.3:n.262-188C>T