Canonical Allele Identifier: CA657663490
Gene: TMPRSS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42389094G>T , CM000683.2:g.42389094G>T GRCh38
NC_000021.8:g.43809203G>T , CM000683.1:g.43809203G>T GRCh37
NC_000021.7:g.42682272G>T NCBI36
NG_011629.1:g.11998C>A
NG_011629.2:g.11998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.206-49C>A ENSP00000411013.3:n.206-49C>A
ENST00000644384.2:c.206-49C>A MANE Select ENSP00000494414.1:n.206-49C>A
ENST00000652415.1:c.206-49C>A ENSP00000498756.1:n.206-49C>A
ENST00000291532.7:c.206-49C>A ENSP00000291532.3:n.206-49C>A
ENST00000398397.3:c.206-49C>A ENSP00000381434.3:n.206-49C>A
ENST00000398405.5:c.200-49C>A ENSP00000381442.1:n.200-49C>A
ENST00000433957.6:c.206-49C>A ENSP00000411013.2:n.206-49C>A
ENST00000474596.5:n.25C>A
ENST00000482761.1:n.493-49C>A
NM_001256317.1:c.206-49C>A NP_001243246.1:n.206-49C>A
NM_024022.2:c.206-49C>A NP_076927.1:n.206-49C>A
NM_032404.2:c.-225C>A NP_115780.1:n.-225C>A
NM_032405.1:c.206-49C>A NP_115781.1:n.206-49C>A
NR_046020.1:n.1162-49C>A
NM_001256317.2:c.206-49C>A NP_001243246.1:n.206-49C>A
NM_024022.3:c.206-49C>A NP_076927.1:n.206-49C>A
NM_032405.2:c.206-49C>A NP_115781.1:n.206-49C>A
NM_001256317.3:c.206-49C>A MANE Select NP_001243246.1:n.206-49C>A
NM_024022.4:c.206-49C>A NP_076927.1:n.206-49C>A
NM_032404.3:c.-225C>A NP_115780.1:n.-225C>A