Canonical Allele Identifier: CA2654681373
Gene: TMPRSS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42390053A>G , CM000683.2:g.42390053A>G GRCh38
NC_000021.8:g.43810162A>G , CM000683.1:g.43810162A>G GRCh37
NC_000021.7:g.42683231A>G NCBI36
NG_011629.1:g.11039T>C
NG_011629.2:g.11039T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.95-16T>C ENSP00000411013.3:n.95-16T>C
ENST00000644384.2:c.95-16T>C MANE Select ENSP00000494414.1:n.95-16T>C
ENST00000652415.1:c.95-16T>C ENSP00000498756.1:n.95-16T>C
ENST00000291532.7:c.95-16T>C ENSP00000291532.3:n.95-16T>C
ENST00000398397.3:c.95-16T>C ENSP00000381434.3:n.95-16T>C
ENST00000398405.5:c.95-22T>C ENSP00000381442.1:n.95-22T>C
ENST00000433957.6:c.95-16T>C ENSP00000411013.2:n.95-16T>C
ENST00000482761.1:n.366T>C
NM_001256317.1:c.95-16T>C NP_001243246.1:n.95-16T>C
NM_024022.2:c.95-16T>C NP_076927.1:n.95-16T>C
NM_032405.1:c.95-16T>C NP_115781.1:n.95-16T>C
NR_046020.1:n.1051-16T>C
NM_001256317.2:c.95-16T>C NP_001243246.1:n.95-16T>C
NM_024022.3:c.95-16T>C NP_076927.1:n.95-16T>C
NM_032405.2:c.95-16T>C NP_115781.1:n.95-16T>C
NM_001256317.3:c.95-16T>C MANE Select NP_001243246.1:n.95-16T>C
NM_024022.4:c.95-16T>C NP_076927.1:n.95-16T>C