Canonical Allele Identifier: CA439641586

Gene: TMPRSS11A

Linked Data

• MyVariant Identifiers: chr4:g.68797713C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67931995C>G , CM000666.2:g.67931995C>G	GRCh38
NC_000004.11:g.68797713C>G , CM000666.1:g.68797713C>G	GRCh37
NC_000004.10:g.68480308C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.318G>C MANE Select	ENSP00000426911.2:p.Leu106=
ENST00000334830.11:c.327G>C	ENSP00000334611.7:p.Leu109=
ENST00000396188.3:c.318G>C	ENSP00000379491.3:p.Leu106=
ENST00000508048.5:c.318G>C	ENSP00000426911.2:p.Leu106=
ENST00000513536.5:c.258G>C	ENSP00000427621.1:p.Leu86=
NM_001114387.1:c.318G>C	NP_001107859.1:p.Leu106=
NM_182606.3:c.327G>C	NP_872412.3:p.Leu109=
NM_001114387.2:c.318G>C MANE Select	NP_001107859.1:p.Leu106=
NM_182606.4:c.327G>C	NP_872412.3:p.Leu109=