Canonical Allele Identifier: CA410374119
Gene: TMPRSS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.43804088G>A (hg19) chr21:g.42383979G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42383979G>A , CM000683.2:g.42383979G>A GRCh38
NC_000021.8:g.43804088G>A , CM000683.1:g.43804088G>A GRCh37
NC_000021.7:g.42677157G>A NCBI36
NG_011629.1:g.17113C>T
NG_011629.2:g.17113C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.607C>T ENSP00000411013.3:p.Gln203Ter
ENST00000644384.2:c.607C>T MANE Select ENSP00000494414.1:p.Gln203Ter
ENST00000652415.1:c.607C>T ENSP00000498756.1:p.Gln203Ter
ENST00000291532.7:c.607C>T ENSP00000291532.3:p.Gln203Ter
ENST00000398397.3:c.607C>T ENSP00000381434.3:p.Gln203Ter
ENST00000398405.5:c.601C>T ENSP00000381442.1:p.Gln201Ter
ENST00000433957.6:c.607C>T ENSP00000411013.2:p.Gln203Ter
ENST00000474596.5:n.475C>T
ENST00000482761.1:n.894C>T
NM_001256317.1:c.607C>T NP_001243246.1:p.Gln203Ter
NM_024022.2:c.607C>T NP_076927.1:p.Gln203Ter
NM_032404.2:c.226C>T NP_115780.1:p.Gln76Ter
NM_032405.1:c.607C>T NP_115781.1:p.Gln203Ter
NR_046020.1:n.1563C>T
NM_001256317.2:c.607C>T NP_001243246.1:p.Gln203Ter
NM_024022.3:c.607C>T NP_076927.1:p.Gln203Ter
NM_032405.2:c.607C>T NP_115781.1:p.Gln203Ter
NM_001256317.3:c.607C>T MANE Select NP_001243246.1:p.Gln203Ter
NM_024022.4:c.607C>T NP_076927.1:p.Gln203Ter
NM_032404.3:c.226C>T NP_115780.1:p.Gln76Ter
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