Canonical Allele Identifier: CA2838481464
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42388568G>A , CM000683.2:g.42388568G>A GRCh38
NC_000021.8:g.43808677G>A , CM000683.1:g.43808677G>A GRCh37
NC_000021.7:g.42681746G>A NCBI36
NG_011629.1:g.12524C>T
NG_011629.2:g.12524C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.323-42C>T ENSP00000411013.3:n.323-42C>T
ENST00000644384.2:c.323-42C>T MANE Select ENSP00000494414.1:n.323-42C>T
ENST00000652415.1:c.323-42C>T ENSP00000498756.1:n.323-42C>T
ENST00000291532.7:c.323-42C>T ENSP00000291532.3:n.323-42C>T
ENST00000398397.3:c.323-42C>T ENSP00000381434.3:n.323-42C>T
ENST00000398405.5:c.317-42C>T ENSP00000381442.1:n.317-42C>T
ENST00000433957.6:c.323-42C>T ENSP00000411013.2:n.323-42C>T
ENST00000474596.5:n.191-42C>T
ENST00000482761.1:n.610-42C>T
NM_001256317.1:c.323-42C>T NP_001243246.1:n.323-42C>T
NM_024022.2:c.323-42C>T NP_076927.1:n.323-42C>T
NM_032404.2:c.-59-42C>T NP_115780.1:n.-59-42C>T
NM_032405.1:c.323-42C>T NP_115781.1:n.323-42C>T
NR_046020.1:n.1279-42C>T
NM_001256317.2:c.323-42C>T NP_001243246.1:n.323-42C>T
NM_024022.3:c.323-42C>T NP_076927.1:n.323-42C>T
NM_032405.2:c.323-42C>T NP_115781.1:n.323-42C>T
NM_001256317.3:c.323-42C>T MANE Select NP_001243246.1:n.323-42C>T
NM_024022.4:c.323-42C>T NP_076927.1:n.323-42C>T
NM_032404.3:c.-59-42C>T NP_115780.1:n.-59-42C>T