Canonical Allele Identifier: CA439641608
Gene: TMPRSS11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68797719G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932001G>C , CM000666.2:g.67932001G>C GRCh38
NC_000004.11:g.68797719G>C , CM000666.1:g.68797719G>C GRCh37
NC_000004.10:g.68480314G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.312C>G MANE Select ENSP00000426911.2:p.Val104=
ENST00000334830.11:c.321C>G ENSP00000334611.7:p.Val107=
ENST00000396188.3:c.312C>G ENSP00000379491.3:p.Val104=
ENST00000508048.5:c.312C>G ENSP00000426911.2:p.Val104=
ENST00000513536.5:c.252C>G ENSP00000427621.1:p.Val84=
NM_001114387.1:c.312C>G NP_001107859.1:p.Val104=
NM_182606.3:c.321C>G NP_872412.3:p.Val107=
NM_001114387.2:c.312C>G MANE Select NP_001107859.1:p.Val104=
NM_182606.4:c.321C>G NP_872412.3:p.Val107=
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