Canonical Allele Identifier: CA439641753
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67932037-T-C
MyVariant Identifiers: chr4:g.68797755T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932037T>C , CM000666.2:g.67932037T>C GRCh38
NC_000004.11:g.68797755T>C , CM000666.1:g.68797755T>C GRCh37
NC_000004.10:g.68480350T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.276A>G MANE Select ENSP00000426911.2:p.Ser92=
ENST00000334830.11:c.285A>G ENSP00000334611.7:p.Ser95=
ENST00000396188.3:c.276A>G ENSP00000379491.3:p.Ser92=
ENST00000508048.5:c.276A>G ENSP00000426911.2:p.Ser92=
ENST00000513536.5:c.216A>G ENSP00000427621.1:p.Ser72=
NM_001114387.1:c.276A>G NP_001107859.1:p.Ser92=
NM_182606.3:c.285A>G NP_872412.3:p.Ser95=
NM_001114387.2:c.276A>G MANE Select NP_001107859.1:p.Ser92=
NM_182606.4:c.285A>G NP_872412.3:p.Ser95=
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