Canonical Allele Identifier: CA357064395

Gene: TMPRSS11A

Linked Data

• MyVariant Identifiers: chr4:g.68797721C>A (hg19) ; chr4:g.67932003C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932003C>A , CM000666.2:g.67932003C>A	GRCh38
NC_000004.11:g.68797721C>A , CM000666.1:g.68797721C>A	GRCh37
NC_000004.10:g.68480316C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.310G>T MANE Select	ENSP00000426911.2:p.Val104Phe
ENST00000334830.11:c.319G>T	ENSP00000334611.7:p.Val107Phe
ENST00000396188.3:c.310G>T	ENSP00000379491.3:p.Val104Phe
ENST00000508048.5:c.310G>T	ENSP00000426911.2:p.Val104Phe
ENST00000513536.5:c.250G>T	ENSP00000427621.1:p.Val84Phe
NM_001114387.1:c.310G>T	NP_001107859.1:p.Val104Phe
NM_182606.3:c.319G>T	NP_872412.3:p.Val107Phe
NM_001114387.2:c.310G>T MANE Select	NP_001107859.1:p.Val104Phe
NM_182606.4:c.319G>T	NP_872412.3:p.Val107Phe