Canonical Allele Identifier: CA357064498
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67932035-G-T
MyVariant Identifiers: chr4:g.68797753G>T (hg19) chr4:g.67932035G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932035G>T , CM000666.2:g.67932035G>T GRCh38
NC_000004.11:g.68797753G>T , CM000666.1:g.68797753G>T GRCh37
NC_000004.10:g.68480348G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.278C>A MANE Select ENSP00000426911.2:p.Ala93Asp
ENST00000334830.11:c.287C>A ENSP00000334611.7:p.Ala96Asp
ENST00000396188.3:c.278C>A ENSP00000379491.3:p.Ala93Asp
ENST00000508048.5:c.278C>A ENSP00000426911.2:p.Ala93Asp
ENST00000513536.5:c.218C>A ENSP00000427621.1:p.Ala73Asp
NM_001114387.1:c.278C>A NP_001107859.1:p.Ala93Asp
NM_182606.3:c.287C>A NP_872412.3:p.Ala96Asp
NM_001114387.2:c.278C>A MANE Select NP_001107859.1:p.Ala93Asp
NM_182606.4:c.287C>A NP_872412.3:p.Ala96Asp
Search 100 bp 5'
Search 100 bp 3'