Canonical Allele Identifier: CA439641763
Gene: TMPRSS11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68797758A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932040A>G , CM000666.2:g.67932040A>G GRCh38
NC_000004.11:g.68797758A>G , CM000666.1:g.68797758A>G GRCh37
NC_000004.10:g.68480353A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.273T>C MANE Select ENSP00000426911.2:p.Asp91=
ENST00000334830.11:c.282T>C ENSP00000334611.7:p.Asp94=
ENST00000396188.3:c.273T>C ENSP00000379491.3:p.Asp91=
ENST00000508048.5:c.273T>C ENSP00000426911.2:p.Asp91=
ENST00000513536.5:c.213T>C ENSP00000427621.1:p.Asp71=
NM_001114387.1:c.273T>C NP_001107859.1:p.Asp91=
NM_182606.3:c.282T>C NP_872412.3:p.Asp94=
NM_001114387.2:c.273T>C MANE Select NP_001107859.1:p.Asp91=
NM_182606.4:c.282T>C NP_872412.3:p.Asp94=