Canonical Allele Identifier: CA512423910
Gene: TMPRSS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43809078T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42388969T>G , CM000683.2:g.42388969T>G GRCh38
NC_000021.8:g.43809078T>G , CM000683.1:g.43809078T>G GRCh37
NC_000021.7:g.42682147T>G NCBI36
NG_011629.1:g.12123A>C
NG_011629.2:g.12123A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.282A>C ENSP00000411013.3:p.Gly94=
ENST00000644384.2:c.282A>C MANE Select ENSP00000494414.1:p.Gly94=
ENST00000652415.1:c.282A>C ENSP00000498756.1:p.Gly94=
ENST00000291532.7:c.282A>C ENSP00000291532.3:p.Gly94=
ENST00000398397.3:c.282A>C ENSP00000381434.3:p.Gly94=
ENST00000398405.5:c.276A>C ENSP00000381442.1:p.Gly92=
ENST00000433957.6:c.282A>C ENSP00000411013.2:p.Gly94=
ENST00000474596.5:n.150A>C
ENST00000482761.1:n.569A>C
NM_001256317.1:c.282A>C NP_001243246.1:p.Gly94=
NM_024022.2:c.282A>C NP_076927.1:p.Gly94=
NM_032404.2:c.-100A>C NP_115780.1:n.-100A>C
NM_032405.1:c.282A>C NP_115781.1:p.Gly94=
NR_046020.1:n.1238A>C
NM_001256317.2:c.282A>C NP_001243246.1:p.Gly94=
NM_024022.3:c.282A>C NP_076927.1:p.Gly94=
NM_032405.2:c.282A>C NP_115781.1:p.Gly94=
NM_001256317.3:c.282A>C MANE Select NP_001243246.1:p.Gly94=
NM_024022.4:c.282A>C NP_076927.1:p.Gly94=
NM_032404.3:c.-100A>C NP_115780.1:n.-100A>C